Canonical Allele Identifier: CA377672964
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942191G>T , CM000672.2:g.94942191G>T GRCh38
NC_000010.10:g.96701948G>T , CM000672.1:g.96701948G>T GRCh37
NC_000010.9:g.96691938G>T NCBI36
NG_008385.1:g.8534G>T
NG_008385.2:g.9034G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.332-1G>T MANE Select ENSP00000260682.6:p.=
ENST00000643112.1:c.332-1G>T ENSP00000496202.1:p.=
ENST00000645207.1:n.485-1G>T
ENST00000260682.6:c.332-1G>T ENSP00000260682.6:p.=
ENST00000461906.1:n.357-1G>T
ENST00000473496.1:n.103-1G>T
NM_000771.3:c.332-1G>T NP_000762.2:p.=
NM_000771.4:c.332-1G>T MANE Select NP_000762.2:p.=