Canonical Allele Identifier: CA211693999
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs975546150
gnomAD v2: 10-96702384-T-G
gnomAD v3: 10-94942627-T-G
gnomAD v4: 10-94942627-T-G
MyVariant Identifiers: chr10:g.96702384T>G (hg19) chr10:g.94942627T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942627T>G , CM000672.2:g.94942627T>G GRCh38
NC_000010.10:g.96702384T>G , CM000672.1:g.96702384T>G GRCh37
NC_000010.9:g.96692374T>G NCBI36
NG_008385.1:g.8970T>G
NG_008385.2:g.9470T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+286T>G MANE Select ENSP00000260682.6:n.481+286T>G
ENST00000643112.1:c.481+286T>G ENSP00000496202.1:n.481+286T>G
ENST00000645207.1:n.634+286T>G
ENST00000260682.6:c.481+286T>G ENSP00000260682.6:n.481+286T>G
ENST00000461906.1:n.792T>G
ENST00000473496.1:n.252+286T>G
NM_000771.3:c.481+286T>G NP_000762.2:n.481+286T>G
NM_000771.4:c.481+286T>G MANE Select NP_000762.2:n.481+286T>G
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