Canonical Allele Identifier: CA5616949
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs767942291
ExAC: 10:96701574 A / C
gnomAD v2: 10-96701574-A-C
gnomAD v4: 10-94941817-A-C
MyVariant Identifiers: chr10:g.96701574A>C (hg19) chr10:g.94941817A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941817A>C , CM000672.2:g.94941817A>C GRCh38
NC_000010.10:g.96701574A>C , CM000672.1:g.96701574A>C GRCh37
NC_000010.9:g.96691564A>C NCBI36
NG_008385.1:g.8160A>C
NG_008385.2:g.8660A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-41A>C MANE Select ENSP00000260682.6:n.169-41A>C
ENST00000643112.1:c.169-41A>C ENSP00000496202.1:n.169-41A>C
ENST00000645207.1:n.281A>C
ENST00000260682.6:c.169-41A>C ENSP00000260682.6:n.169-41A>C
ENST00000461906.1:n.194-41A>C
NM_000771.3:c.169-41A>C NP_000762.2:n.169-41A>C
NM_000771.4:c.169-41A>C MANE Select NP_000762.2:n.169-41A>C
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