Linked Data
MyVariant Identifiers:
chr2:g.31751262T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31526192T>G , CM000664.2:g.31526192T>G | GRCh38 |
| NC_000002.11:g.31751262T>G , CM000664.1:g.31751262T>G | GRCh37 |
| NC_000002.10:g.31604766T>G | NCBI36 |
| NG_008365.1:g.59780A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000622030.2:c.*4A>C MANE Select | ENSP00000477587.1:n.*4A>C | |
| ENST00000622030.1:c.*4A>C | ENSP00000477587.1:n.*4A>C | |
| NM_000348.3:c.*4A>C | NP_000339.2:n.*4A>C | |
| XM_011533069.1:c.*4A>C | XP_011531371.1:n.*4A>C | |
| XM_011533070.1:c.*4A>C | XP_011531372.1:n.*4A>C | |
| XM_011533071.1:c.*4A>C | XP_011531373.1:n.*4A>C | |
| XM_011533072.1:c.*4A>C | XP_011531374.1:n.*4A>C | |
| XM_011533069.2:c.*4A>C | XP_011531371.1:n.*4A>C | |
| XM_011533072.2:c.*4A>C | XP_011531374.1:n.*4A>C | |
| NM_000348.4:c.*4A>C MANE Select | NP_000339.2:n.*4A>C |