Linked Data
ClinVar Variation Id:
437775
ClinVar RCV Id:
RCV000503754
dbSNP Id:
rs748236641
ExAC:
6:99323413 C / A
gnomAD v2:
6-99323413-C-A
gnomAD v3:
6-98875537-C-A
gnomAD v4:
6-98875537-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98875537C>A , CM000668.2:g.98875537C>A | GRCh38 |
| NC_000006.11:g.99323413C>A , CM000668.1:g.99323413C>A | GRCh37 |
| NC_000006.10:g.99430134C>A | NCBI36 |
| NG_033903.1:g.77470G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369244.7:c.1580G>T MANE Select | ENSP00000358247.1:p.Arg527Ile | |
| ENST00000229971.2:c.1580G>T | ENSP00000229971.1:p.Arg527Ile | |
| ENST00000369244.6:c.1580G>T | ENSP00000358247.1:p.Arg527Ile | |
| NM_001278716.1:c.1580G>T | NP_001265645.1:p.Arg527Ile | |
| NM_012160.4:c.1580G>T | NP_036292.2:p.Arg527Ile | |
| NR_103836.1:n.1625G>T | ||
| XM_005266930.1:c.1508G>T | XP_005266987.1:p.Arg503Ile | |
| XM_005266930.3:c.1508G>T | XP_005266987.1:p.Arg503Ile | |
| XM_017010726.1:c.1580G>T | XP_016866215.1:p.Arg527Ile | |
| XM_017010727.2:c.1508G>T | XP_016866216.1:p.Arg503Ile | |
| XM_017010728.1:c.854G>T | XP_016866217.1:p.Arg285Ile | |
| NM_001278716.2:c.1580G>T MANE Select | NP_001265645.1:p.Arg527Ile | |
| NR_103836.2:n.1565G>T | ||
| NM_012160.5:c.1580G>T | NP_036292.2:p.Arg527Ile |