Canonical Allele Identifier: CA377677129
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748742C>A (hg19) chr10:g.94988985C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988985C>A , CM000672.2:g.94988985C>A GRCh38
NC_000010.10:g.96748742C>A , CM000672.1:g.96748742C>A GRCh37
NC_000010.9:g.96738732C>A NCBI36
NG_008385.1:g.55328C>A
NG_008385.2:g.55828C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1430C>A MANE Select ENSP00000260682.6:p.Ala477Asp
ENST00000643112.1:c.*439C>A ENSP00000496202.1:n.*439C>A
ENST00000260682.6:c.1430C>A ENSP00000260682.6:p.Ala477Asp
NM_000771.3:c.1430C>A NP_000762.2:p.Ala477Asp
NM_000771.4:c.1430C>A MANE Select NP_000762.2:p.Ala477Asp
Search 100 bp 5'
Search 100 bp 3'