Canonical Allele Identifier: CA211724687
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1022002707
gnomAD v2: 10-96734288-T-G
gnomAD v3: 10-94974531-T-G
gnomAD v4: 10-94974531-T-G
MyVariant Identifiers: chr10:g.96734288T>G (hg19) chr10:g.94974531T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974531T>G , CM000672.2:g.94974531T>G GRCh38
NC_000010.10:g.96734288T>G , CM000672.1:g.96734288T>G GRCh37
NC_000010.9:g.96724278T>G NCBI36
NG_008385.1:g.40874T>G
NG_008385.2:g.41374T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.961+2286T>G MANE Select ENSP00000260682.6:n.961+2286T>G
ENST00000643112.1:c.820-6652T>G ENSP00000496202.1:n.820-6652T>G
ENST00000260682.6:c.961+2286T>G ENSP00000260682.6:n.961+2286T>G
NM_000771.3:c.961+2286T>G NP_000762.2:n.961+2286T>G
NM_000771.4:c.961+2286T>G MANE Select NP_000762.2:n.961+2286T>G
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