Linked Data
dbSNP Id:
rs768300290
ExAC:
7:42005479 G / A
gnomAD v2:
7-42005479-G-A
gnomAD v4:
7-41965881-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41965881G>A , CM000669.2:g.41965881G>A | GRCh38 |
| NC_000007.13:g.42005479G>A , CM000669.1:g.42005479G>A | GRCh37 |
| NC_000007.12:g.41972004G>A | NCBI36 |
| NG_008434.1:g.276140C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.3192C>T MANE Select | ENSP00000379258.3:p.Pro1064= | |
| ENST00000677288.1:c.3018C>T | ENSP00000503986.1:p.Pro1006= | |
| ENST00000677605.1:c.3192C>T | ENSP00000503743.1:p.Pro1064= | |
| ENST00000678429.1:c.3192C>T | ENSP00000502957.1:p.Pro1064= | |
| ENST00000395925.7:c.3192C>T | ENSP00000379258.3:p.Pro1064= | |
| ENST00000479210.1:n.3169C>T | ||
| NM_000168.5:c.3192C>T | NP_000159.3:p.Pro1064= | |
| XM_005249703.1:c.3192C>T | XP_005249760.1:p.Pro1064= | |
| XM_005249704.2:c.3192C>T | XP_005249761.1:p.Pro1064= | |
| XM_011515272.1:c.3192C>T | XP_011513574.1:p.Pro1064= | |
| XM_011515273.1:c.3192C>T | XP_011513575.1:p.Pro1064= | |
| XM_011515274.1:c.3015C>T | XP_011513576.1:p.Pro1005= | |
| XM_011515274.2:c.3015C>T | XP_011513576.1:p.Pro1005= | |
| XM_017011997.1:c.3189C>T | XP_016867486.1:p.Pro1063= | |
| NM_000168.6:c.3192C>T MANE Select | NP_000159.3:p.Pro1064= |