Canonical Allele Identifier: CA13311819
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs28371675
gnomAD v2: 10-96702337-C-T
gnomAD v3: 10-94942580-C-T
gnomAD v4: 10-94942580-C-T
MyVariant Identifiers: chr10:g.96702337C>T (hg19) chr10:g.94942580C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942580C>T , CM000672.2:g.94942580C>T GRCh38
NC_000010.10:g.96702337C>T , CM000672.1:g.96702337C>T GRCh37
NC_000010.9:g.96692327C>T NCBI36
NG_008385.1:g.8923C>T
NG_008385.2:g.9423C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+239C>T MANE Select ENSP00000260682.6:n.481+239C>T
ENST00000643112.1:c.481+239C>T ENSP00000496202.1:n.481+239C>T
ENST00000645207.1:n.634+239C>T
ENST00000260682.6:c.481+239C>T ENSP00000260682.6:n.481+239C>T
ENST00000461906.1:n.745C>T
ENST00000473496.1:n.252+239C>T
NM_000771.3:c.481+239C>T NP_000762.2:n.481+239C>T
NM_000771.4:c.481+239C>T MANE Select NP_000762.2:n.481+239C>T
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