Canonical Allele Identifier: CA5617308
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs781370526
ExAC: 10:96741069 C / T
gnomAD v2: 10-96741069-C-T
gnomAD v4: 10-94981312-C-T
COSMIC: COSM4902697
MyVariant Identifiers: chr10:g.96741069C>T (hg19) chr10:g.94981312C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981312C>T , CM000672.2:g.94981312C>T GRCh38
NC_000010.10:g.96741069C>T , CM000672.1:g.96741069C>T GRCh37
NC_000010.9:g.96731059C>T NCBI36
NG_008385.1:g.47655C>T
NG_008385.2:g.48155C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1091C>T MANE Select ENSP00000260682.6:p.Thr364Ile
ENST00000643112.1:c.*100C>T ENSP00000496202.1:n.*100C>T
ENST00000260682.6:c.1091C>T ENSP00000260682.6:p.Thr364Ile
NM_000771.3:c.1091C>T NP_000762.2:p.Thr364Ile
NM_000771.4:c.1091C>T MANE Select NP_000762.2:p.Thr364Ile
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