Canonical Allele Identifier: CA2610267785
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94942156-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94942156G>C , CM000672.2:g.94942156G>C GRCh38
NC_000010.10:g.96701913G>C , CM000672.1:g.96701913G>C GRCh37
NC_000010.9:g.96691903G>C NCBI36
NG_008385.1:g.8499G>C
NG_008385.2:g.8999G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.332-36G>C MANE Select ENSP00000260682.6:n.332-36G>C
ENST00000643112.1:c.332-36G>C ENSP00000496202.1:n.332-36G>C
ENST00000645207.1:n.485-36G>C
ENST00000260682.6:c.332-36G>C ENSP00000260682.6:n.332-36G>C
ENST00000461906.1:n.357-36G>C
ENST00000473496.1:n.103-36G>C
NM_000771.3:c.332-36G>C NP_000762.2:n.332-36G>C
NM_000771.4:c.332-36G>C MANE Select NP_000762.2:n.332-36G>C
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