HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115732902C>G , CM000663.2:g.115732902C>G | GRCh38 |
NC_000001.10:g.116275523C>G , CM000663.1:g.116275523C>G | GRCh37 |
NC_000001.9:g.116077046C>G | NCBI36 |
NG_008802.1:g.40904G>C , LRG_404:g.40904G>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000488931.2:c.329G>C | ENSP00000518226.1:p.Gly110Ala | |
ENST00000261448.6:c.605G>C MANE Select | ENSP00000261448.5:p.Gly202Ala | |
ENST00000261448.5:c.605G>C | ENSP00000261448.5:p.Gly202Ala | |
ENST00000488931.1:n.26G>C | ||
NM_001232.3:c.605G>C , LRG_404t1:c.605G>C | NP_001223.2:p.Gly202Ala | |
NM_001232.4:c.605G>C MANE Select | NP_001223.2:p.Gly202Ala |