Linked Data
dbSNP Id:
rs1008119386
gnomAD v3:
2-70831576-C-T
gnomAD v4:
2-70831576-C-T
MyVariant Identifiers:
chr2:g.70831576C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.70831576C>T , CM000664.2:g.70831576C>T | GRCh38 |
| NC_000002.11:g.71058707C>T , CM000664.1:g.71058707C>T | GRCh37 |
| NC_000002.10:g.70912215C>T | NCBI36 |
| NG_033914.1:g.9248G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000410009.5:c.836+125G>A MANE Select | ENSP00000386378.3:n.836+125G>A | |
| ENST00000410009.4:c.836+125G>A | ENSP00000386378.3:n.836+125G>A | |
| NM_015717.4:c.836+125G>A | NP_056532.4:n.836+125G>A | |
| XM_011532874.1:c.836+125G>A | XP_011531176.1:n.836+125G>A | |
| XM_011532875.1:c.836+125G>A | XP_011531177.1:n.836+125G>A | |
| XM_011532876.1:c.836+125G>A | XP_011531178.1:n.836+125G>A | |
| XM_011532875.2:c.836+125G>A | XP_011531177.1:n.836+125G>A | |
| XM_011532876.2:c.836+125G>A | XP_011531178.1:n.836+125G>A | |
| NM_015717.5:c.836+125G>A MANE Select | NP_056532.4:n.836+125G>A |