Canonical Allele Identifier: CA2580976031
Gene: CYP2C9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942097C>G , CM000672.2:g.94942097C>G GRCh38
NC_000010.10:g.96701854C>G , CM000672.1:g.96701854C>G GRCh37
NC_000010.9:g.96691844C>G NCBI36
NG_008385.1:g.8440C>G
NG_008385.2:g.8940C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.331+77C>G MANE Select ENSP00000260682.6:n.331+77C>G
ENST00000643112.1:c.331+77C>G ENSP00000496202.1:n.331+77C>G
ENST00000645207.1:n.484+77C>G
ENST00000260682.6:c.331+77C>G ENSP00000260682.6:n.331+77C>G
ENST00000461906.1:n.356+77C>G
ENST00000473496.1:n.102+77C>G
NM_000771.3:c.331+77C>G NP_000762.2:n.331+77C>G
NM_000771.4:c.331+77C>G MANE Select NP_000762.2:n.331+77C>G