Linked Data
gnomAD v3:
3-98585619-G-T
gnomAD v4:
3-98585619-G-T
MyVariant Identifiers:
chr3:g.98304463G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.98585619G>T , CM000665.2:g.98585619G>T | GRCh38 |
| NC_000003.11:g.98304463G>T , CM000665.1:g.98304463G>T | GRCh37 |
| NC_000003.10:g.99787153G>T | NCBI36 |
| NG_015994.1:g.12993C>A | |
| NG_015994.2:g.12993C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647941.2:c.994C>A MANE Select | ENSP00000497326.1:p.Arg332= | |
| ENST00000264193.2:c.994C>A | ENSP00000264193.2:p.Arg332= | |
| ENST00000510489.1:n.244C>A | ||
| NM_000097.5:c.994C>A | NP_000088.3:p.Arg332= | |
| XM_005247125.3:c.994C>A | XP_005247182.1:p.Arg332= | |
| NM_000097.7:c.994C>A MANE Select | NP_000088.3:p.Arg332= | |
| XM_005247125.4:c.994C>A | XP_005247182.1:p.Arg332= | |
| XR_001740025.2:n.1165C>A | ||
| XR_001740026.1:n.1729C>A | ||
| XR_001740027.1:n.1269C>A | ||
| XR_001740028.1:n.1235C>A |