Canonical Allele Identifier: CA377673958

Gene: CYP2C9

Linked Data

• MyVariant Identifiers: chr10:g.96708871A>T (hg19) ; chr10:g.94949114A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94949114A>T , CM000672.2:g.94949114A>T	GRCh38
NC_000010.10:g.96708871A>T , CM000672.1:g.96708871A>T	GRCh37
NC_000010.9:g.96698861A>T	NCBI36
NG_008385.1:g.15457A>T
NG_008385.2:g.15957A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.649A>T MANE Select	ENSP00000260682.6:p.Asn217Tyr
ENST00000643112.1:c.649A>T	ENSP00000496202.1:p.Asn217Tyr
ENST00000260682.6:c.649A>T	ENSP00000260682.6:p.Asn217Tyr
ENST00000473496.1:n.420A>T
NM_000771.3:c.649A>T	NP_000762.2:p.Asn217Tyr
NM_000771.4:c.649A>T MANE Select	NP_000762.2:p.Asn217Tyr