HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189008952G>C , CM000664.2:g.189008952G>C | GRCh38 |
NC_000002.11:g.189873678G>C , CM000664.1:g.189873678G>C | GRCh37 |
NC_000002.10:g.189581923G>C | NCBI36 |
NG_007404.1:g.39580G>C , LRG_3:g.39580G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.3455G>C | ENSP00000415346.2:p.Gly1152Ala | |
ENST00000304636.9:c.3554G>C MANE Select | ENSP00000304408.4:p.Gly1185Ala | |
ENST00000304636.7:c.3554G>C | ENSP00000304408.3:p.Gly1185Ala | |
ENST00000317840.9:c.2645G>C | ENSP00000315243.6:p.Gly882Ala | |
ENST00000487010.1:n.651G>C | ||
NM_000090.3:c.3554G>C , LRG_3t1:c.3554G>C | NP_000081.1:p.Gly1185Ala | |
NM_000090.4:c.3554G>C MANE Select | NP_000081.2:p.Gly1185Ala |