Canonical Allele Identifier: CA1373743937
Gene:

Linked Data

dbSNP Id: rs1701574338

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577145del , CM000665.2:g.70577145del GRCh38
NC_000003.11:g.70626296del , CM000665.1:g.70626296del GRCh37
NC_000003.10:g.70708986del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1192del
XR_001740559.1:n.367-1192del