HGVS | Genome Assembly |
---|---|
NC_000001.11:g.159886676G>C , CM000663.2:g.159886676G>C | GRCh38 |
NC_000001.10:g.159856466G>C , CM000663.1:g.159856466G>C | GRCh37 |
NC_000001.9:g.158123090G>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368099.9:c.602C>G MANE Select | ENSP00000357079.4:p.Ala201Gly | |
ENST00000368099.8:c.602C>G | ENSP00000357079.4:p.Ala201Gly | |
ENST00000426543.6:c.347C>G | ENSP00000403044.2:p.Ala116Gly | |
ENST00000476696.5:c.602C>G | ENSP00000483972.1:p.Ala201Gly | |
ENST00000479940.2:c.347C>G | ENSP00000478944.1:p.Ala116Gly | |
NM_012337.2:c.602C>G | NP_036469.2:p.Ala201Gly | |
NM_012337.3:c.602C>G MANE Select | NP_036469.2:p.Ala201Gly |