Canonical Allele Identifier: CA470987391
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96701755T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941998T>A , CM000672.2:g.94941998T>A GRCh38
NC_000010.10:g.96701755T>A , CM000672.1:g.96701755T>A GRCh37
NC_000010.9:g.96691745T>A NCBI36
NG_008385.1:g.8341T>A
NG_008385.2:g.8841T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.309T>A MANE Select ENSP00000260682.6:p.Ala103=
ENST00000643112.1:c.309T>A ENSP00000496202.1:p.Ala103=
ENST00000645207.1:n.462T>A
ENST00000260682.6:c.309T>A ENSP00000260682.6:p.Ala103=
ENST00000461906.1:n.334T>A
ENST00000473496.1:n.80T>A
NM_000771.3:c.309T>A NP_000762.2:p.Ala103=
NM_000771.4:c.309T>A MANE Select NP_000762.2:p.Ala103=
Search 100 bp 5'
Search 100 bp 3'