Canonical Allele Identifier: CA918431513
Gene:

Linked Data

dbSNP Id: rs1586967739

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551327del , CM000671.2:g.25551327del GRCh38
NC_000009.11:g.25551325del , CM000671.1:g.25551325del GRCh37
NC_000009.10:g.25541325del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_929525.1:n.50-755del
XR_929525.2:n.674-755del