Linked Data
ClinVar Variation Id:
160349
dbSNP Id:
rs199756983
ExAC:
8:42977872 T / A
gnomAD v2:
8-42977872-T-A
gnomAD v3:
8-43122729-T-A
gnomAD v4:
8-43122729-T-A
PubMed:
PMID:24925318
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.43122729T>A , CM000670.2:g.43122729T>A | GRCh38 |
| NC_000008.10:g.42977872T>A , CM000670.1:g.42977872T>A | GRCh37 |
| NC_000008.9:g.43097029T>A | NCBI36 |
| NG_033235.1:g.34224T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000331373.10:c.905T>A MANE Select | ENSP00000331258.5:p.Val302Asp | |
| ENST00000614426.2:c.*701T>A | ENSP00000478821.2:n.*701T>A | |
| ENST00000674646.1:c.623T>A | ENSP00000501703.1:p.Val208Asp | |
| ENST00000674676.1:c.623T>A | ENSP00000502544.1:p.Val208Asp | |
| ENST00000674782.1:c.*825T>A | ENSP00000501683.1:n.*825T>A | |
| ENST00000674937.1:c.863T>A | ENSP00000501823.1:p.Val288Asp | |
| ENST00000675322.1:c.623T>A | ENSP00000502235.1:p.Val208Asp | |
| ENST00000675675.1:c.623T>A | ENSP00000501793.1:p.Val208Asp | |
| ENST00000676178.1:c.*690T>A | ENSP00000502007.1:n.*690T>A | |
| ENST00000676193.1:c.905T>A | ENSP00000502774.1:p.Val302Asp | |
| ENST00000331373.9:c.905T>A | ENSP00000331258.5:p.Val302Asp | |
| ENST00000614426.1:c.905T>A | ENSP00000478821.1:p.Val302Asp | |
| NM_001277971.1:c.905T>A | NP_001264900.1:p.Val302Asp | |
| NM_032237.4:c.905T>A | NP_115613.1:p.Val302Asp | |
| XM_011544668.1:c.905T>A | XP_011542970.1:p.Val302Asp | |
| XM_011544669.1:c.905T>A | XP_011542971.1:p.Val302Asp | |
| NM_032237.5:c.905T>A MANE Select | NP_115613.1:p.Val302Asp | |
| NM_001277971.2:c.905T>A | NP_001264900.1:p.Val302Asp |