Linked Data
ClinVar Variation Id:
14106
dbSNP Id:
rs121913639
gnomAD v4:
14-23424026-C-T
PubMed:
PMID:7909436
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23424026C>T , CM000676.2:g.23424026C>T | GRCh38 |
| NC_000014.8:g.23893235C>T , CM000676.1:g.23893235C>T | GRCh37 |
| NC_000014.7:g.22963075C>T | NCBI36 |
| NG_007884.1:g.16636G>A , LRG_384:g.16636G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355349.4:c.2803G>A MANE Select | ENSP00000347507.3:p.Glu935Lys | |
| ENST00000355349.3:c.2803G>A | ENSP00000347507.3:p.Glu935Lys | |
| NM_000257.3:c.2803G>A | NP_000248.2:p.Glu935Lys | |
| XR_245686.3:n.2909G>A | ||
| XM_017021340.1:c.2803G>A | XP_016876829.1:p.Glu935Lys | |
| NM_000257.4:c.2803G>A MANE Select | NP_000248.2:p.Glu935Lys |