Canonical Allele Identifier: CA377673952
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949112G>C , CM000672.2:g.94949112G>C GRCh38
NC_000010.10:g.96708869G>C , CM000672.1:g.96708869G>C GRCh37
NC_000010.9:g.96698859G>C NCBI36
NG_008385.1:g.15455G>C
NG_008385.2:g.15955G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.647G>C MANE Select ENSP00000260682.6:p.Cys216Ser
ENST00000643112.1:c.647G>C ENSP00000496202.1:p.Cys216Ser
ENST00000260682.6:c.647G>C ENSP00000260682.6:p.Cys216Ser
ENST00000473496.1:n.418G>C
NM_000771.3:c.647G>C NP_000762.2:p.Cys216Ser
NM_000771.4:c.647G>C MANE Select NP_000762.2:p.Cys216Ser