Linked Data
ClinVar Variation Id:
3659
ClinVar RCV Id:
RCV000003844
dbSNP Id:
rs121908049
gnomAD v4:
16-67940471-G-T
PubMed:
PMID:1681161
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.67940471G>T , CM000678.2:g.67940471G>T | GRCh38 |
| NC_000016.9:g.67974374G>T , CM000678.1:g.67974374G>T | GRCh37 |
| NC_000016.8:g.66531875G>T | NCBI36 |
| NG_009778.1:g.8642C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264005.10:c.756C>A MANE Select | ENSP00000264005.5:p.Asn252Lys | |
| ENST00000264005.9:c.756C>A | ENSP00000264005.5:p.Asn252Lys | |
| ENST00000570369.5:c.156-397C>A | ||
| ENST00000570980.1:c.540C>A | ENSP00000464651.1:p.Asn180Lys | |
| ENST00000573538.5:c.494C>A | ENSP00000463220.1:n.494C>A | |
| NM_000229.1:c.756C>A | NP_000220.1:p.Asn252Lys | |
| NM_000229.2:c.756C>A MANE Select | NP_000220.1:p.Asn252Lys |