Canonical Allele Identifier: CA670187901
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1223006109

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989040T>C , CM000672.2:g.94989040T>C GRCh38
NC_000010.10:g.96748797T>C , CM000672.1:g.96748797T>C GRCh37
NC_000010.9:g.96738787T>C NCBI36
NG_008385.1:g.55383T>C
NG_008385.2:g.55883T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*12T>C MANE Select ENSP00000260682.6:n.*12T>C
ENST00000643112.1:c.*494T>C ENSP00000496202.1:n.*494T>C
ENST00000260682.6:c.*12T>C ENSP00000260682.6:n.*12T>C
NM_000771.3:c.*12T>C NP_000762.2:n.*12T>C
NM_000771.4:c.*12T>C MANE Select NP_000762.2:n.*12T>C