Canonical Allele Identifier: CA470832613
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96708867C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949110C>T , CM000672.2:g.94949110C>T GRCh38
NC_000010.10:g.96708867C>T , CM000672.1:g.96708867C>T GRCh37
NC_000010.9:g.96698857C>T NCBI36
NG_008385.1:g.15453C>T
NG_008385.2:g.15953C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.645C>T MANE Select ENSP00000260682.6:p.Ile215=
ENST00000643112.1:c.645C>T ENSP00000496202.1:p.Ile215=
ENST00000260682.6:c.645C>T ENSP00000260682.6:p.Ile215=
ENST00000473496.1:n.416C>T
NM_000771.3:c.645C>T NP_000762.2:p.Ile215=
NM_000771.4:c.645C>T MANE Select NP_000762.2:p.Ile215=
Search 100 bp 5'
Search 100 bp 3'