Canonical Allele Identifier: CA1247519033
Gene:

Linked Data

dbSNP Id: rs1667989865

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534524_41534536del , CM000664.2:g.41534524_41534536del GRCh38
NC_000002.11:g.41761664_41761676del , CM000664.1:g.41761664_41761676del GRCh37
NC_000002.10:g.41615168_41615180del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939996.1:n.181+3194_181+3206del
XR_939997.1:n.146+3194_146+3206del
XR_939997.2:n.9529+3194_9529+3206del