Linked Data
dbSNP Id:
rs2034143
gnomAD v2:
8-6310738-A-C
gnomAD v3:
8-6453217-A-C
gnomAD v4:
8-6453217-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.6453217A>C , CM000670.2:g.6453217A>C | GRCh38 |
| NC_000008.10:g.6310738A>C , CM000670.1:g.6310738A>C | GRCh37 |
| NC_000008.9:g.6298146A>C | NCBI36 |
| NG_016619.1:g.51626A>C | |
| NG_016619.2:g.51626A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000687720.1:c.*1774-1926A>C | ENSP00000510728.1:n.*1774-1926A>C | |
| ENST00000687874.1:n.686-1926A>C | ||
| ENST00000688101.1:c.1246-1926A>C | ||
| ENST00000688388.1:c.1826-1926A>C | ENSP00000510092.1:n.1826-1926A>C | |
| ENST00000688658.1:n.666-1926A>C | ||
| ENST00000688912.1:n.1837-1926A>C | ||
| ENST00000689348.1:c.1826-1926A>C | ENSP00000509554.1:n.1826-1926A>C | |
| ENST00000689633.1:c.1826-1926A>C | ENSP00000509054.1:n.1826-1926A>C | |
| ENST00000689736.1:c.671-1926A>C | ENSP00000509722.1:n.671-1926A>C | |
| ENST00000690159.1:c.*2105-1926A>C | ENSP00000510482.1:n.*2105-1926A>C | |
| ENST00000690708.1:c.671-1926A>C | ENSP00000510400.1:n.671-1926A>C | |
| ENST00000690826.1:c.1826-1926A>C | ENSP00000510536.1:n.1826-1926A>C | |
| ENST00000691435.1:c.1826-1926A>C | ENSP00000510652.1:n.1826-1926A>C | |
| ENST00000691655.1:c.*681-1926A>C | ENSP00000509652.1:n.*681-1926A>C | |
| ENST00000692534.1:c.204-1926A>C | ||
| ENST00000692836.1:c.1826-1926A>C | ENSP00000509971.1:n.1826-1926A>C | |
| ENST00000692938.1:c.1826-1926A>C | ENSP00000509072.1:n.1826-1926A>C | |
| ENST00000693231.1:c.*1566-1926A>C | ENSP00000510764.1:n.*1566-1926A>C | |
| ENST00000693528.1:n.59-1926A>C | ||
| ENST00000344683.10:c.1826-1926A>C MANE Select | ENSP00000342924.5:n.1826-1926A>C | |
| ENST00000344683.9:c.1826-1926A>C | ENSP00000342924.5:n.1826-1926A>C | |
| NM_024596.3:c.1826-1926A>C | NP_078872.2:n.1826-1926A>C | |
| XM_011534755.1:c.1826-1926A>C | XP_011533057.1:n.1826-1926A>C | |
| XM_011534756.1:c.1826-1926A>C | XP_011533058.1:n.1826-1926A>C | |
| XM_011534757.1:c.1826-1926A>C | XP_011533059.1:n.1826-1926A>C | |
| XM_011534758.1:c.1826-1926A>C | XP_011533060.1:n.1826-1926A>C | |
| XM_011534759.1:c.1826-1926A>C | XP_011533061.1:n.1826-1926A>C | |
| XM_011534760.1:c.1301-1926A>C | XP_011533062.1:n.1301-1926A>C | |
| NM_001322042.1:c.1826-1926A>C | NP_001308971.1:n.1826-1926A>C | |
| NM_001363979.1:c.1826-1926A>C | NP_001350908.1:n.1826-1926A>C | |
| NM_001363980.1:c.1826-1926A>C | NP_001350909.1:n.1826-1926A>C | |
| NM_024596.4:c.1826-1926A>C | NP_078872.2:n.1826-1926A>C | |
| XM_011534755.3:c.1826-1926A>C | XP_011533057.1:n.1826-1926A>C | |
| XM_011534756.3:c.1826-1926A>C | XP_011533058.1:n.1826-1926A>C | |
| XM_011534757.3:c.1826-1926A>C | XP_011533059.1:n.1826-1926A>C | |
| XM_011534758.3:c.1826-1926A>C | XP_011533060.1:n.1826-1926A>C | |
| XM_011534759.3:c.1826-1926A>C | XP_011533061.1:n.1826-1926A>C | |
| XM_011534760.2:c.1301-1926A>C | XP_011533062.1:n.1301-1926A>C | |
| XM_017013829.2:c.1826-1926A>C | XP_016869318.1:n.1826-1926A>C | |
| XM_017013831.2:c.1826-1926A>C | XP_016869320.1:n.1826-1926A>C | |
| XM_017013832.2:c.1826-1926A>C | XP_016869321.1:n.1826-1926A>C | |
| XM_017013833.2:c.1826-1926A>C | XP_016869322.1:n.1826-1926A>C | |
| XR_001745596.2:n.1879-1926A>C | ||
| NM_024596.5:c.1826-1926A>C MANE Select | NP_078872.3:n.1826-1926A>C | |
| NM_001322042.2:c.1826-1926A>C | NP_001308971.2:n.1826-1926A>C | |
| NM_001363980.2:c.1826-1926A>C | NP_001350909.1:n.1826-1926A>C |