Linked Data
MyVariant Identifiers:
chr3:g.119132819A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119413972A>C , CM000665.2:g.119413972A>C | GRCh38 |
| NC_000003.11:g.119132819A>C , CM000665.1:g.119132819A>C | GRCh37 |
| NC_000003.10:g.120615509A>C | NCBI36 |
| NG_007665.2:g.124600A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2043A>C MANE Select | ENSP00000264245.4:p.Pro681= | |
| ENST00000264245.8:c.2043A>C | ENSP00000264245.4:p.Pro681= | |
| NM_020754.3:c.2043A>C | NP_065805.2:p.Pro681= | |
| XM_005247671.3:c.1950A>C | XP_005247728.1:p.Pro650= | |
| XM_006713714.2:c.1983A>C | XP_006713777.1:p.Pro661= | |
| XM_006713714.3:c.1983A>C | XP_006713777.1:p.Pro661= | |
| XM_017006955.1:c.1551A>C | XP_016862444.1:p.Pro517= | |
| NM_020754.4:c.2043A>C MANE Select | NP_065805.2:p.Pro681= |