Linked Data
MyVariant Identifiers:
chr2:g.71058855T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.70831724T>G , CM000664.2:g.70831724T>G | GRCh38 |
| NC_000002.11:g.71058855T>G , CM000664.1:g.71058855T>G | GRCh37 |
| NC_000002.10:g.70912363T>G | NCBI36 |
| NG_033914.1:g.9100A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000410009.5:c.813A>C MANE Select | ENSP00000386378.3:p.Pro271= | |
| ENST00000410009.4:c.813A>C | ENSP00000386378.3:p.Pro271= | |
| NM_015717.4:c.813A>C | NP_056532.4:p.Pro271= | |
| XM_011532874.1:c.813A>C | XP_011531176.1:p.Pro271= | |
| XM_011532875.1:c.813A>C | XP_011531177.1:p.Pro271= | |
| XM_011532876.1:c.813A>C | XP_011531178.1:p.Pro271= | |
| XM_011532875.2:c.813A>C | XP_011531177.1:p.Pro271= | |
| XM_011532876.2:c.813A>C | XP_011531178.1:p.Pro271= | |
| NM_015717.5:c.813A>C MANE Select | NP_056532.4:p.Pro271= |