Canonical Allele Identifier: CA377673948
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96708868T>A (hg19) chr10:g.94949111T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949111T>A , CM000672.2:g.94949111T>A GRCh38
NC_000010.10:g.96708868T>A , CM000672.1:g.96708868T>A GRCh37
NC_000010.9:g.96698858T>A NCBI36
NG_008385.1:g.15454T>A
NG_008385.2:g.15954T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.646T>A MANE Select ENSP00000260682.6:p.Cys216Ser
ENST00000643112.1:c.646T>A ENSP00000496202.1:p.Cys216Ser
ENST00000260682.6:c.646T>A ENSP00000260682.6:p.Cys216Ser
ENST00000473496.1:n.417T>A
NM_000771.3:c.646T>A NP_000762.2:p.Cys216Ser
NM_000771.4:c.646T>A MANE Select NP_000762.2:p.Cys216Ser
Search 100 bp 5'
Search 100 bp 3'