Linked Data
MyVariant Identifiers:
chr3:g.14170929C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14129429C>A , CM000665.2:g.14129429C>A | GRCh38 |
| NC_000003.11:g.14170929C>A , CM000665.1:g.14170929C>A | GRCh37 |
| NC_000003.10:g.14145930C>A | NCBI36 |
| NG_008975.1:g.9490C>A , LRG_435:g.9490C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*60C>A | ENSP00000395617.1:n.*60C>A | |
| ENST00000306077.5:c.30C>A MANE Select | ENSP00000303992.5:p.Thr10= | |
| ENST00000306077.4:c.30C>A | ENSP00000303992.4:p.Thr10= | |
| ENST00000432444.1:c.*60C>A | ENSP00000395617.1:n.*60C>A | |
| NM_024334.2:c.30C>A , LRG_435t1:c.30C>A | NP_077310.1:p.Thr10= | |
| XM_011534109.1:c.-76C>A | XP_011532411.1:n.-76C>A | |
| XM_017007176.2:c.-76C>A | XP_016862665.1:n.-76C>A | |
| NM_024334.3:c.30C>A MANE Select | NP_077310.1:p.Thr10= |