Canonical Allele Identifier: CA595638882
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1463737634

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989036C>T , CM000672.2:g.94989036C>T GRCh38
NC_000010.10:g.96748793C>T , CM000672.1:g.96748793C>T GRCh37
NC_000010.9:g.96738783C>T NCBI36
NG_008385.1:g.55379C>T
NG_008385.2:g.55879C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*8C>T MANE Select ENSP00000260682.6:n.*8C>T
ENST00000643112.1:c.*490C>T ENSP00000496202.1:n.*490C>T
ENST00000260682.6:c.*8C>T ENSP00000260682.6:n.*8C>T
NM_000771.3:c.*8C>T NP_000762.2:n.*8C>T
NM_000771.4:c.*8C>T MANE Select NP_000762.2:n.*8C>T