Canonical Allele Identifier: CA2574622597
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94988776-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988776A>T , CM000672.2:g.94988776A>T GRCh38
NC_000010.10:g.96748533A>T , CM000672.1:g.96748533A>T GRCh37
NC_000010.9:g.96738523A>T NCBI36
NG_008385.1:g.55119A>T
NG_008385.2:g.55619A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000260682.8:c.1292-71A>T MANE Select ENSP00000260682.6:n.1292-71A>T
ENST00000643112.1:c.*301-71A>T ENSP00000496202.1:n.*301-71A>T
ENST00000260682.6:c.1292-71A>T ENSP00000260682.6:n.1292-71A>T
NM_000771.3:c.1292-71A>T NP_000762.2:n.1292-71A>T
NM_000771.4:c.1292-71A>T MANE Select NP_000762.2:n.1292-71A>T
Search 100 bp 5'
Search 100 bp 3'