Canonical Allele Identifier: CA1439212879
Gene:

Linked Data

dbSNP Id: rs1711589923

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578248_12578249del , CM000666.2:g.12578248_12578249del GRCh38
NC_000004.11:g.12579872_12579873del , CM000666.1:g.12579872_12579873del GRCh37
NC_000004.10:g.12188970_12188971del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31094_106+31095del
XR_001741374.1:n.254+44407_254+44408del
XR_925406.3:n.140+31094_140+31095del