Canonical Allele Identifier: CA595314685
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1340379178
gnomAD v2: 10-96701509-GC-G
gnomAD v3: 10-94941752-GC-G
gnomAD v4: 10-94941752-GC-G
MyVariant Identifiers: chr10:g.96701510del (hg19) chr10:g.94941753del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94941753del , CM000672.2:g.94941753del GRCh38
NC_000010.10:g.96701510del , CM000672.1:g.96701510del GRCh37
NC_000010.9:g.96691500del NCBI36
NG_008385.1:g.8096del
NG_008385.2:g.8596del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.169-105del MANE Select ENSP00000260682.6:n.169-105del
ENST00000643112.1:c.169-105del ENSP00000496202.1:n.169-105del
ENST00000645207.1:n.217del
ENST00000260682.6:c.169-105del ENSP00000260682.6:n.169-105del
ENST00000461906.1:n.194-105del
NM_000771.3:c.169-105del NP_000762.2:n.169-105del
NM_000771.4:c.169-105del MANE Select NP_000762.2:n.169-105del
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