Canonical Allele Identifier: CA670183198
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1432053591
gnomAD v3: 10-94981590-C-G
gnomAD v4: 10-94981590-C-G
MyVariant Identifiers: chr10:g.96741347C>G (hg19) chr10:g.94981590C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94981590C>G , CM000672.2:g.94981590C>G GRCh38
NC_000010.10:g.96741347C>G , CM000672.1:g.96741347C>G GRCh37
NC_000010.9:g.96731337C>G NCBI36
NG_008385.1:g.47933C>G
NG_008385.2:g.48433C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1149+220C>G MANE Select ENSP00000260682.6:n.1149+220C>G
ENST00000643112.1:c.*158+220C>G ENSP00000496202.1:n.*158+220C>G
ENST00000260682.6:c.1149+220C>G ENSP00000260682.6:n.1149+220C>G
NM_000771.3:c.1149+220C>G NP_000762.2:n.1149+220C>G
NM_000771.4:c.1149+220C>G MANE Select NP_000762.2:n.1149+220C>G
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