Linked Data
ClinVar Variation Id:
1452485
ClinVar RCV Id:
RCV001999832
dbSNP Id:
rs2152011135
gnomAD v4:
6-42722273-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42722273C>T , CM000668.2:g.42722273C>T | GRCh38 |
| NC_000006.11:g.42690011C>T , CM000668.1:g.42690011C>T | GRCh37 |
| NC_000006.10:g.42797989C>T | NCBI36 |
| NG_009176.1:g.5348G>A | |
| NG_009176.2:g.5348G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.62G>A MANE Select | ENSP00000230381.5:p.Trp21Ter | |
| ENST00000230381.6:c.62G>A | ENSP00000230381.5:p.Trp21Ter | |
| NM_000322.4:c.62G>A | NP_000313.2:p.Trp21Ter | |
| XR_427834.2:n.717G>A | ||
| XR_926295.1:n.717G>A | ||
| XR_427834.4:n.767G>A | ||
| XR_926295.3:n.767G>A | ||
| NM_000322.5:c.62G>A MANE Select | NP_000313.2:p.Trp21Ter |