Canonical Allele Identifier: CA211698552
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs980559074
MyVariant Identifiers: chr10:g.96707320T>C (hg19) chr10:g.94947563T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94947563T>C , CM000672.2:g.94947563T>C GRCh38
NC_000010.10:g.96707320T>C , CM000672.1:g.96707320T>C GRCh37
NC_000010.9:g.96697310T>C NCBI36
NG_008385.1:g.13906T>C
NG_008385.2:g.14406T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.482-216T>C MANE Select ENSP00000260682.6:n.482-216T>C
ENST00000643112.1:c.482-216T>C ENSP00000496202.1:n.482-216T>C
ENST00000645207.1:n.635-216T>C
ENST00000260682.6:c.482-216T>C ENSP00000260682.6:n.482-216T>C
ENST00000473496.1:n.253-216T>C
NM_000771.3:c.482-216T>C NP_000762.2:n.482-216T>C
NM_000771.4:c.482-216T>C MANE Select NP_000762.2:n.482-216T>C
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