Canonical Allele Identifier: CA670236178
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1188942869
MyVariant Identifiers: chr10:g.96701780A>G (hg19) chr10:g.94942023A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942023A>G , CM000672.2:g.94942023A>G GRCh38
NC_000010.10:g.96701780A>G , CM000672.1:g.96701780A>G GRCh37
NC_000010.9:g.96691770A>G NCBI36
NG_008385.1:g.8366A>G
NG_008385.2:g.8866A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.331+3A>G MANE Select ENSP00000260682.6:n.331+3A>G
ENST00000643112.1:c.331+3A>G ENSP00000496202.1:n.331+3A>G
ENST00000645207.1:n.484+3A>G
ENST00000260682.6:c.331+3A>G ENSP00000260682.6:n.331+3A>G
ENST00000461906.1:n.356+3A>G
ENST00000473496.1:n.102+3A>G
NM_000771.3:c.331+3A>G NP_000762.2:n.331+3A>G
NM_000771.4:c.331+3A>G MANE Select NP_000762.2:n.331+3A>G
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