Canonical Allele Identifier: CA670235935
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1231271444
MyVariant Identifiers: chr10:g.96701528A>C (hg19) chr10:g.94941771A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941771A>C , CM000672.2:g.94941771A>C GRCh38
NC_000010.10:g.96701528A>C , CM000672.1:g.96701528A>C GRCh37
NC_000010.9:g.96691518A>C NCBI36
NG_008385.1:g.8114A>C
NG_008385.2:g.8614A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-87A>C MANE Select ENSP00000260682.6:n.169-87A>C
ENST00000643112.1:c.169-87A>C ENSP00000496202.1:n.169-87A>C
ENST00000645207.1:n.235A>C
ENST00000260682.6:c.169-87A>C ENSP00000260682.6:n.169-87A>C
ENST00000461906.1:n.194-87A>C
NM_000771.3:c.169-87A>C NP_000762.2:n.169-87A>C
NM_000771.4:c.169-87A>C MANE Select NP_000762.2:n.169-87A>C
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