Canonical Allele Identifier: CA595638879
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1426917768
gnomAD v2: 10-96740896-C-G
MyVariant Identifiers: chr10:g.96740896C>G (hg19) chr10:g.94981139C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981139C>G , CM000672.2:g.94981139C>G GRCh38
NC_000010.10:g.96740896C>G , CM000672.1:g.96740896C>G GRCh37
NC_000010.9:g.96730886C>G NCBI36
NG_008385.1:g.47482C>G
NG_008385.2:g.47982C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.962-44C>G MANE Select ENSP00000260682.6:n.962-44C>G
ENST00000643112.1:c.820-44C>G ENSP00000496202.1:n.820-44C>G
ENST00000260682.6:c.962-44C>G ENSP00000260682.6:n.962-44C>G
NM_000771.3:c.962-44C>G NP_000762.2:n.962-44C>G
NM_000771.4:c.962-44C>G MANE Select NP_000762.2:n.962-44C>G
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