Canonical Allele Identifier: CA211735745
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs943396313
gnomAD v3: 10-94989085-G-C
gnomAD v4: 10-94989085-G-C
MyVariant Identifiers: chr10:g.96748842G>C (hg19) chr10:g.94989085G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989085G>C , CM000672.2:g.94989085G>C GRCh38
NC_000010.10:g.96748842G>C , CM000672.1:g.96748842G>C GRCh37
NC_000010.9:g.96738832G>C NCBI36
NG_008385.1:g.55428G>C
NG_008385.2:g.55928G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*57G>C MANE Select ENSP00000260682.6:n.*57G>C
ENST00000643112.1:c.*539G>C ENSP00000496202.1:n.*539G>C
ENST00000260682.6:c.*57G>C ENSP00000260682.6:n.*57G>C
NM_000771.3:c.*57G>C NP_000762.2:n.*57G>C
NM_000771.4:c.*57G>C MANE Select NP_000762.2:n.*57G>C
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