Linked Data
ClinVar Variation Id:
2019856
ClinVar RCV Id:
RCV002852132
gnomAD v4:
3-32997225-C-T
MyVariant Identifiers:
chr3:g.33038717C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.32997225C>T , CM000665.2:g.32997225C>T | GRCh38 |
| NC_000003.11:g.33038717C>T , CM000665.1:g.33038717C>T | GRCh37 |
| NC_000003.10:g.33013721C>T | NCBI36 |
| NG_009005.1:g.104978G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.1854G>A MANE Select | ENSP00000306920.4:p.Val618= | |
| ENST00000307363.9:c.1854G>A | ENSP00000306920.4:p.Val618= | |
| ENST00000307377.12:c.1461G>A | ENSP00000305920.8:p.Val487= | |
| ENST00000399402.7:c.1764G>A | ENSP00000382333.2:p.Val588= | |
| NM_000404.2:c.1854G>A | NP_000395.2:p.Val618= | |
| NM_000404.3:c.1854G>A | NP_000395.2:p.Val618= | |
| NM_001079811.1:c.1764G>A | NP_001073279.1:p.Val588= | |
| NM_001079811.2:c.1764G>A | NP_001073279.1:p.Val588= | |
| NM_001135602.1:c.1461G>A | NP_001129074.1:p.Val487= | |
| NM_001135602.2:c.1461G>A | NP_001129074.1:p.Val487= | |
| NM_001317040.1:c.1998G>A | NP_001303969.1:p.Val666= | |
| NM_000404.4:c.1854G>A MANE Select | NP_000395.3:p.Val618= | |
| NM_001079811.3:c.1764G>A | NP_001073279.2:p.Val588= | |
| NM_001135602.3:c.1461G>A | NP_001129074.2:p.Val487= | |
| NM_001317040.2:c.1998G>A | NP_001303969.2:p.Val666= | |
| NM_001393580.1:c.1734+16831G>A | NP_001380509.1:n.1734+16831G>A |