Canonical Allele Identifier: CA2705173451
Gene:

Linked Data

dbSNP Id: rs2108921702

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578291_12578292del , CM000666.2:g.12578291_12578292del GRCh38
NC_000004.11:g.12579915_12579916del , CM000666.1:g.12579915_12579916del GRCh37
NC_000004.10:g.12189013_12189014del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31052_106+31053del
XR_001741374.1:n.254+44365_254+44366del
XR_925406.3:n.140+31052_140+31053del