Canonical Allele Identifier: CA377674339
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96709038G>C (hg19) chr10:g.94949281G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949281G>C , CM000672.2:g.94949281G>C GRCh38
NC_000010.10:g.96709038G>C , CM000672.1:g.96709038G>C GRCh37
NC_000010.9:g.96699028G>C NCBI36
NG_008385.1:g.15624G>C
NG_008385.2:g.16124G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.816G>C MANE Select ENSP00000260682.6:p.Glu272Asp
ENST00000643112.1:c.816G>C ENSP00000496202.1:p.Glu272Asp
ENST00000260682.6:c.816G>C ENSP00000260682.6:p.Glu272Asp
ENST00000473496.1:n.587G>C
NM_000771.3:c.816G>C NP_000762.2:p.Glu272Asp
NM_000771.4:c.816G>C MANE Select NP_000762.2:p.Glu272Asp
Search 100 bp 5'
Search 100 bp 3'