Linked Data
ClinVar Variation Id:
2717080
ClinVar RCV Id:
RCV003548624
dbSNP Id:
rs749407558
gnomAD v2:
2-44104775-G-A
gnomAD v3:
2-43877636-G-A
gnomAD v4:
2-43877636-G-A
COSMIC:
COSM1408151
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43877636G>A , CM000664.2:g.43877636G>A | GRCh38 |
| NC_000002.11:g.44104775G>A , CM000664.1:g.44104775G>A | GRCh37 |
| NC_000002.10:g.43958279G>A | NCBI36 |
| NG_008884.1:g.43673G>A | |
| NG_008884.2:g.50695G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272286.4:c.1832G>A MANE Select | ENSP00000272286.2:p.Arg611Lys | |
| ENST00000272286.2:c.1832G>A | ENSP00000272286.2:p.Arg611Lys | |
| NM_022437.2:c.1832G>A | NP_071882.1:p.Arg611Lys | |
| XM_005264483.2:c.1829G>A | XP_005264540.1:p.Arg610Lys | |
| XM_011533029.1:c.1844G>A | XP_011531331.1:p.Arg615Lys | |
| XM_011533030.1:c.1841G>A | XP_011531332.1:p.Arg614Lys | |
| XM_011533031.1:c.1616G>A | XP_011531333.1:p.Arg539Lys | |
| XR_939707.1:n.2334G>A | ||
| NM_001357321.1:c.1829G>A | NP_001344250.1:p.Arg610Lys | |
| XM_011533029.2:c.1844G>A | XP_011531331.1:p.Arg615Lys | |
| XM_011533030.2:c.1841G>A | XP_011531332.1:p.Arg614Lys | |
| XR_001738891.1:n.2348G>A | ||
| XR_939707.2:n.2348G>A | ||
| NM_022437.3:c.1832G>A MANE Select | NP_071882.1:p.Arg611Lys | |
| NM_001357321.2:c.1829G>A | NP_001344250.1:p.Arg610Lys |