Linked Data
ClinVar Variation Id:
766099
ClinVar RCV Id:
RCV000944595
dbSNP Id:
rs761649200
ExAC:
11:5246998 G / A
gnomAD v2:
11-5246998-G-A
gnomAD v4:
11-5225768-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225768G>A , CM000673.2:g.5225768G>A | GRCh38 |
| NC_000011.9:g.5246998G>A , CM000673.1:g.5246998G>A | GRCh37 |
| NC_000011.8:g.5203574G>A | NCBI36 |
| NG_000007.3:g.71848C>T | |
| NG_059281.1:g.6304C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.316-42C>T | ENSP00000494175.1:n.316-42C>T | |
| ENST00000335295.4:c.316-42C>T MANE Select | ENSP00000333994.3:n.316-42C>T | |
| ENST00000475226.1:n.248-42C>T | ||
| ENST00000633227.1:c.*132-42C>T | ENSP00000488004.1:n.*132-42C>T | |
| NM_000518.4:c.316-42C>T | NP_000509.1:n.316-42C>T | |
| NM_000518.5:c.316-42C>T MANE Select | NP_000509.1:n.316-42C>T |