Canonical Allele Identifier: CA2610266889
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94989156-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94989156G>A , CM000672.2:g.94989156G>A GRCh38
NC_000010.10:g.96748913G>A , CM000672.1:g.96748913G>A GRCh37
NC_000010.9:g.96738903G>A NCBI36
NG_008385.1:g.55499G>A
NG_008385.2:g.55999G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.*128G>A MANE Select ENSP00000260682.6:n.*128G>A
ENST00000643112.1:c.*610G>A ENSP00000496202.1:n.*610G>A
ENST00000260682.6:c.*128G>A ENSP00000260682.6:n.*128G>A
NM_000771.3:c.*128G>A NP_000762.2:n.*128G>A
NM_000771.4:c.*128G>A MANE Select NP_000762.2:n.*128G>A
Search 100 bp 5'
Search 100 bp 3'