Canonical Allele Identifier: CA931402116
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974516A>T , CM000672.2:g.94974516A>T GRCh38
NC_000010.10:g.96734273A>T , CM000672.1:g.96734273A>T GRCh37
NC_000010.9:g.96724263A>T NCBI36
NG_008385.1:g.40859A>T
NG_008385.2:g.41359A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2271A>T MANE Select ENSP00000260682.6:n.961+2271A>T
ENST00000643112.1:c.820-6667A>T ENSP00000496202.1:n.820-6667A>T
ENST00000260682.6:c.961+2271A>T ENSP00000260682.6:n.961+2271A>T
NM_000771.3:c.961+2271A>T NP_000762.2:n.961+2271A>T
NM_000771.4:c.961+2271A>T MANE Select NP_000762.2:n.961+2271A>T