Canonical Allele Identifier: CA377676906
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96748634C>A (hg19) chr10:g.94988877C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988877C>A , CM000672.2:g.94988877C>A GRCh38
NC_000010.10:g.96748634C>A , CM000672.1:g.96748634C>A GRCh37
NC_000010.9:g.96738624C>A NCBI36
NG_008385.1:g.55220C>A
NG_008385.2:g.55720C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1322C>A MANE Select ENSP00000260682.6:p.Ala441Asp
ENST00000643112.1:c.*331C>A ENSP00000496202.1:n.*331C>A
ENST00000260682.6:c.1322C>A ENSP00000260682.6:p.Ala441Asp
NM_000771.3:c.1322C>A NP_000762.2:p.Ala441Asp
NM_000771.4:c.1322C>A MANE Select NP_000762.2:p.Ala441Asp
Search 100 bp 5'
Search 100 bp 3'