Canonical Allele Identifier: CA670178333
Gene: CYP2C9 HGNC NCBI

Linked Data

dbSNP Id: rs1209227970
gnomAD v3: 10-94974446-A-AT
gnomAD v4: 10-94974446-A-AT
MyVariant Identifiers: chr10:g.96734203_96734204insT (hg19) chr10:g.94974446_94974447insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94974452dup , CM000672.2:g.94974452dup GRCh38
NC_000010.10:g.96734209dup , CM000672.1:g.96734209dup GRCh37
NC_000010.9:g.96724199dup NCBI36
NG_008385.1:g.40795dup
NG_008385.2:g.41295dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000260682.8:c.961+2207dup MANE Select ENSP00000260682.6:n.961+2207dup
ENST00000643112.1:c.820-6731dup ENSP00000496202.1:n.820-6731dup
ENST00000260682.6:c.961+2207dup ENSP00000260682.6:n.961+2207dup
NM_000771.3:c.961+2207dup NP_000762.2:n.961+2207dup
NM_000771.4:c.961+2207dup MANE Select NP_000762.2:n.961+2207dup
Search 100 bp 5'
Search 100 bp 3'