Canonical Allele Identifier: CA1929298177
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1589408492
gnomAD v4: 10-94949041-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94949041G>A , CM000672.2:g.94949041G>A GRCh38
NC_000010.10:g.96708798G>A , CM000672.1:g.96708798G>A GRCh37
NC_000010.9:g.96698788G>A NCBI36
NG_008385.1:g.15384G>A
NG_008385.2:g.15884G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.643-67G>A MANE Select ENSP00000260682.6:n.643-67G>A
ENST00000643112.1:c.643-67G>A ENSP00000496202.1:n.643-67G>A
ENST00000260682.6:c.643-67G>A ENSP00000260682.6:n.643-67G>A
ENST00000473496.1:n.414-67G>A
NM_000771.3:c.643-67G>A NP_000762.2:n.643-67G>A
NM_000771.4:c.643-67G>A MANE Select NP_000762.2:n.643-67G>A
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