Linked Data
gnomAD v4:
8-54626390-G-T
COSMIC:
COSM3374954
MyVariant Identifiers:
chr8:g.55538950G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.54626390G>T , CM000670.2:g.54626390G>T | GRCh38 |
| NC_000008.10:g.55538950G>T , CM000670.1:g.55538950G>T | GRCh37 |
| NC_000008.9:g.55701503G>T | NCBI36 |
| NG_009840.1:g.15324G>T | |
| NG_009840.2:g.15324G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220676.2:c.2508G>T MANE Select | ENSP00000220676.1:p.Pro836= | |
| ENST00000636932.1:c.787+4102G>T | ENSP00000489857.1:n.787+4102G>T | |
| ENST00000637698.1:c.787+4102G>T | ENSP00000490104.1:n.787+4102G>T | |
| ENST00000220676.1:c.2508G>T | ENSP00000220676.1:p.Pro836= | |
| NM_006269.1:c.2508G>T | NP_006260.1:p.Pro836= | |
| XM_017013721.1:c.2529G>T | XP_016869210.1:p.Pro843= | |
| XM_017013722.1:c.2508G>T | XP_016869211.1:p.Pro836= | |
| NM_001375654.1:c.787+4102G>T | NP_001362583.1:n.787+4102G>T | |
| NM_006269.2:c.2508G>T MANE Select | NP_006260.1:p.Pro836= |