Canonical Allele Identifier: CA377673994
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96708887T>A (hg19) chr10:g.94949130T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949130T>A , CM000672.2:g.94949130T>A GRCh38
NC_000010.10:g.96708887T>A , CM000672.1:g.96708887T>A GRCh37
NC_000010.9:g.96698877T>A NCBI36
NG_008385.1:g.15473T>A
NG_008385.2:g.15973T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.665T>A MANE Select ENSP00000260682.6:p.Ile222Asn
ENST00000643112.1:c.665T>A ENSP00000496202.1:p.Ile222Asn
ENST00000260682.6:c.665T>A ENSP00000260682.6:p.Ile222Asn
ENST00000473496.1:n.436T>A
NM_000771.3:c.665T>A NP_000762.2:p.Ile222Asn
NM_000771.4:c.665T>A MANE Select NP_000762.2:p.Ile222Asn
Search 100 bp 5'
Search 100 bp 3'