HGVS | Genome Assembly |
---|---|
NC_000004.12:g.52027969G>C , CM000666.2:g.52027969G>C | GRCh38 |
NC_000004.11:g.52894135G>C , CM000666.1:g.52894135G>C | GRCh37 |
NC_000004.10:g.52588892G>C | NCBI36 |
NG_008891.1:g.15351C>G , LRG_204:g.15351C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000381431.10:c.752C>G MANE Select | ENSP00000370839.6:p.Ala251Gly | |
ENST00000381431.9:c.752C>G | ENSP00000370839.5:p.Ala251Gly | |
NM_000232.4:c.752C>G , LRG_204t1:c.752C>G | NP_000223.1:p.Ala251Gly | |
XM_006714049.2:c.455C>G | XP_006714112.1:p.Ala152Gly | |
XM_011534403.1:c.542C>G | XP_011532705.1:p.Ala181Gly | |
XM_011534404.1:c.455C>G | XP_011532706.1:p.Ala152Gly | |
NM_000232.5:c.752C>G MANE Select | NP_000223.1:p.Ala251Gly |