Canonical Allele Identifier: CA1439212661
Gene:

Linked Data

dbSNP Id: rs1711580837

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578045_12578046del , CM000666.2:g.12578045_12578046del GRCh38
NC_000004.11:g.12579669_12579670del , CM000666.1:g.12579669_12579670del GRCh37
NC_000004.10:g.12188767_12188768del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31297_106+31298del
XR_001741374.1:n.254+44610_254+44611del
XR_925406.3:n.140+31297_140+31298del