Canonical Allele Identifier: CA377677087
Gene: CYP2C9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988963A>T , CM000672.2:g.94988963A>T GRCh38
NC_000010.10:g.96748720A>T , CM000672.1:g.96748720A>T GRCh37
NC_000010.9:g.96738710A>T NCBI36
NG_008385.1:g.55306A>T
NG_008385.2:g.55806A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1408A>T MANE Select ENSP00000260682.6:p.Thr470Ser
ENST00000643112.1:c.*417A>T ENSP00000496202.1:n.*417A>T
ENST00000260682.6:c.1408A>T ENSP00000260682.6:p.Thr470Ser
NM_000771.3:c.1408A>T NP_000762.2:p.Thr470Ser
NM_000771.4:c.1408A>T MANE Select NP_000762.2:p.Thr470Ser