Canonical Allele Identifier: CA670178703
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1368291135
gnomAD v3: 10-94974657-CA-C
gnomAD v4: 10-94974657-CA-C
MyVariant Identifiers: chr10:g.96734415del (hg19) chr10:g.94974658del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974659del , CM000672.2:g.94974659del GRCh38
NC_000010.10:g.96734416del , CM000672.1:g.96734416del GRCh37
NC_000010.9:g.96724406del NCBI36
NG_008385.1:g.41002del
NG_008385.2:g.41502del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2414del MANE Select ENSP00000260682.6:n.961+2414del
ENST00000643112.1:c.820-6524del ENSP00000496202.1:n.820-6524del
ENST00000260682.6:c.961+2414del ENSP00000260682.6:n.961+2414del
NM_000771.3:c.961+2414del NP_000762.2:n.961+2414del
NM_000771.4:c.961+2414del MANE Select NP_000762.2:n.961+2414del
Search 100 bp 5'
Search 100 bp 3'