Canonical Allele Identifier: CA377677096
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748726G>A (hg19) chr10:g.94988969G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988969G>A , CM000672.2:g.94988969G>A GRCh38
NC_000010.10:g.96748726G>A , CM000672.1:g.96748726G>A GRCh37
NC_000010.9:g.96738716G>A NCBI36
NG_008385.1:g.55312G>A
NG_008385.2:g.55812G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1414G>A MANE Select ENSP00000260682.6:p.Val472Ile
ENST00000643112.1:c.*423G>A ENSP00000496202.1:n.*423G>A
ENST00000260682.6:c.1414G>A ENSP00000260682.6:p.Val472Ile
NM_000771.3:c.1414G>A NP_000762.2:p.Val472Ile
NM_000771.4:c.1414G>A MANE Select NP_000762.2:p.Val472Ile
Search 100 bp 5'
Search 100 bp 3'