Canonical Allele Identifier: CA16398898
Gene: CYP2C9 HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.94988735G>A
GRCh37 chr10:g.96748492G>A
gnomAD v2:
10:96748492 G / A
gnomAD v3:
10:94988735 G / A
gnomAD v4:
chr10-94988735-G-A
Joint Max Group AF 0.19232836 (NFE)
Genomes Max Group AF 0.19014582 (NFE)
Exomes Max Group AF 0.192313 (NFE)
dbSNP:
9332238
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988735G>A , CM000672.2:g.94988735G>A GRCh38
NC_000010.10:g.96748492G>A , CM000672.1:g.96748492G>A GRCh37
NC_000010.9:g.96738482G>A NCBI36
NG_008385.1:g.55078G>A
NG_008385.2:g.55578G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-112G>A MANE Select ENSP00000260682.6:n.1292-112G>A
ENST00000643112.1:c.*301-112G>A ENSP00000496202.1:n.*301-112G>A
ENST00000260682.6:c.1292-112G>A ENSP00000260682.6:n.1292-112G>A
NM_000771.3:c.1292-112G>A NP_000762.2:n.1292-112G>A
NM_000771.4:c.1292-112G>A MANE Select NP_000762.2:n.1292-112G>A
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