Canonical Allele Identifier: CA917329464
Gene:

Linked Data

dbSNP Id: rs1560829389

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148748382del , CM000666.2:g.148748382del GRCh38
NC_000004.11:g.149669534del , CM000666.1:g.149669534del GRCh37
NC_000004.10:g.149888984del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741441.1:n.1746-118375del