Canonical Allele Identifier: CA377674134
Gene: CYP2C9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96708950A>C (hg19) chr10:g.94949193A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949193A>C , CM000672.2:g.94949193A>C GRCh38
NC_000010.10:g.96708950A>C , CM000672.1:g.96708950A>C GRCh37
NC_000010.9:g.96698940A>C NCBI36
NG_008385.1:g.15536A>C
NG_008385.2:g.16036A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.728A>C MANE Select ENSP00000260682.6:p.Tyr243Ser
ENST00000643112.1:c.728A>C ENSP00000496202.1:p.Tyr243Ser
ENST00000260682.6:c.728A>C ENSP00000260682.6:p.Tyr243Ser
ENST00000473496.1:n.499A>C
NM_000771.3:c.728A>C NP_000762.2:p.Tyr243Ser
NM_000771.4:c.728A>C MANE Select NP_000762.2:p.Tyr243Ser
Search 100 bp 5'
Search 100 bp 3'