Canonical Allele Identifier: CA867312792
Gene:

Linked Data

dbSNP Id: rs1230634784
MyVariant Identifiers: chr9:g.82345905del (hg19) chr9:g.79730990del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.79730991del , CM000671.2:g.79730991del GRCh38
NC_000009.11:g.82345906del , CM000671.1:g.82345906del GRCh37
NC_000009.10:g.81535726del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929980.1:n.1019+679del
Search 100 bp 5'
Search 100 bp 3'