Linked Data
MyVariant Identifiers:
chr2:g.31748937C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31523867C>A , CM000664.2:g.31523867C>A | GRCh38 |
| NC_000002.11:g.31748937C>A , CM000664.1:g.31748937C>A | GRCh37 |
| NC_000002.10:g.31602441C>A | NCBI36 |
| NG_008365.1:g.62105G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000622030.2:c.*2329G>T MANE Select | ENSP00000477587.1:n.*2329G>T | |
| ENST00000622030.1:c.*2329G>T | ENSP00000477587.1:n.*2329G>T | |
| XM_011533069.1:c.*2329G>T | XP_011531371.1:n.*2329G>T | |
| XM_011533070.1:c.*2329G>T | XP_011531372.1:n.*2329G>T | |
| XM_011533071.1:c.*2329G>T | XP_011531373.1:n.*2329G>T | |
| XM_011533072.1:c.*2329G>T | XP_011531374.1:n.*2329G>T | |
| XM_011533069.2:c.*2329G>T | XP_011531371.1:n.*2329G>T | |
| XM_011533072.2:c.*2329G>T | XP_011531374.1:n.*2329G>T | |
| NM_000348.4:c.*2329G>T MANE Select | NP_000339.2:n.*2329G>T |