Canonical Allele Identifier: CA1929292674
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2031415213
gnomAD v4: 10-94942730-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942730G>A , CM000672.2:g.94942730G>A GRCh38
NC_000010.10:g.96702487G>A , CM000672.1:g.96702487G>A GRCh37
NC_000010.9:g.96692477G>A NCBI36
NG_008385.1:g.9073G>A
NG_008385.2:g.9573G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.481+389G>A MANE Select ENSP00000260682.6:n.481+389G>A
ENST00000643112.1:c.481+389G>A ENSP00000496202.1:n.481+389G>A
ENST00000645207.1:n.634+389G>A
ENST00000260682.6:c.481+389G>A ENSP00000260682.6:n.481+389G>A
ENST00000461906.1:n.895G>A
ENST00000473496.1:n.252+389G>A
NM_000771.3:c.481+389G>A NP_000762.2:n.481+389G>A
NM_000771.4:c.481+389G>A MANE Select NP_000762.2:n.481+389G>A
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