HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64751381C>G , CM000673.2:g.64751381C>G | GRCh38 |
NC_000011.9:g.64518853C>G , CM000673.1:g.64518853C>G | GRCh37 |
NC_000011.8:g.64275429C>G | NCBI36 |
NG_013018.1:g.14335G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.1913G>C MANE Select | ENSP00000164139.3:p.Gly638Ala | |
ENST00000164139.3:c.1913G>C | ENSP00000164139.3:p.Gly638Ala | |
ENST00000377432.7:c.1649G>C | ENSP00000366650.3:p.Gly550Ala | |
ENST00000462303.1:n.237G>C | ||
NM_001164716.1:c.1649G>C | NP_001158188.1:p.Gly550Ala | |
NM_005609.2:c.1913G>C | NP_005600.1:p.Gly638Ala | |
NM_005609.3:c.1913G>C | NP_005600.1:p.Gly638Ala | |
NM_005609.4:c.1913G>C MANE Select | NP_005600.1:p.Gly638Ala |