Canonical Allele Identifier: CA931402030
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs2032096122
gnomAD v3: 10-94974437-A-C
gnomAD v4: 10-94974437-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974437A>C , CM000672.2:g.94974437A>C GRCh38
NC_000010.10:g.96734194A>C , CM000672.1:g.96734194A>C GRCh37
NC_000010.9:g.96724184A>C NCBI36
NG_008385.1:g.40780A>C
NG_008385.2:g.41280A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2192A>C MANE Select ENSP00000260682.6:n.961+2192A>C
ENST00000643112.1:c.820-6746A>C ENSP00000496202.1:n.820-6746A>C
ENST00000260682.6:c.961+2192A>C ENSP00000260682.6:n.961+2192A>C
NM_000771.3:c.961+2192A>C NP_000762.2:n.961+2192A>C
NM_000771.4:c.961+2192A>C MANE Select NP_000762.2:n.961+2192A>C
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