Canonical Allele Identifier: CA2610266721
Gene: CYP2C9 HGNC NCBI

Linked Data

gnomAD v4: 10-94988698-GCACCCATC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94988707_94988714del , CM000672.2:g.94988707_94988714del GRCh38
NC_000010.10:g.96748464_96748471del , CM000672.1:g.96748464_96748471del GRCh37
NC_000010.9:g.96738454_96738461del NCBI36
NG_008385.1:g.55050_55057del
NG_008385.2:g.55550_55557del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.1292-140_1292-133del MANE Select ENSP00000260682.6:n.1292-140_1292-133del
ENST00000643112.1:c.*301-140_*301-133del ENSP00000496202.1:n.*301-140_*301-133del
ENST00000260682.6:c.1292-140_1292-133del ENSP00000260682.6:n.1292-140_1292-133del
NM_000771.3:c.1292-140_1292-133del NP_000762.2:n.1292-140_1292-133del
NM_000771.4:c.1292-140_1292-133del MANE Select NP_000762.2:n.1292-140_1292-133del
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