Canonical Allele Identifier: CA1059429987
Gene:

Linked Data

dbSNP Id: rs1711588495

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578200del , CM000666.2:g.12578200del GRCh38
NC_000004.11:g.12579824del , CM000666.1:g.12579824del GRCh37
NC_000004.10:g.12188922del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31143del
XR_001741374.1:n.254+44456del
XR_925406.3:n.140+31143del