Canonical Allele Identifier: CA2610266846
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94989061-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989061G>C , CM000672.2:g.94989061G>C GRCh38
NC_000010.10:g.96748818G>C , CM000672.1:g.96748818G>C GRCh37
NC_000010.9:g.96738808G>C NCBI36
NG_008385.1:g.55404G>C
NG_008385.2:g.55904G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.*33G>C MANE Select ENSP00000260682.6:n.*33G>C
ENST00000643112.1:c.*515G>C ENSP00000496202.1:n.*515G>C
ENST00000260682.6:c.*33G>C ENSP00000260682.6:n.*33G>C
NM_000771.3:c.*33G>C NP_000762.2:n.*33G>C
NM_000771.4:c.*33G>C MANE Select NP_000762.2:n.*33G>C
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