Canonical Allele Identifier: CA587286156
Gene:

Linked Data

dbSNP Id: rs1387949278

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551295del , CM000671.2:g.25551295del GRCh38
NC_000009.11:g.25551293del , CM000671.1:g.25551293del GRCh37
NC_000009.10:g.25541293del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-719del
XR_929525.2:n.674-719del