Canonical Allele Identifier: CA587286390
Gene:

Linked Data

dbSNP Id: rs1310337038
gnomAD v2: 9-25551488-CTG-C
gnomAD v3: 9-25551490-CTG-C
gnomAD v4: 9-25551490-CTG-C
MyVariant Identifiers: chr9:g.25551489_25551490del (hg19) chr9:g.25551491_25551492del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551492_25551493del , CM000671.2:g.25551492_25551493del GRCh38
NC_000009.11:g.25551490_25551491del , CM000671.1:g.25551490_25551491del GRCh37
NC_000009.10:g.25541490_25541491del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-920_50-919del
XR_929525.2:n.674-920_674-919del
Search 100 bp 5'
Search 100 bp 3'