Canonical Allele Identifier: CA1247519141
Gene:

Linked Data

dbSNP Id: rs1667991860

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534677del , CM000664.2:g.41534677del GRCh38
NC_000002.11:g.41761817del , CM000664.1:g.41761817del GRCh37
NC_000002.10:g.41615321del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3049del
XR_939997.1:n.146+3049del
XR_939997.2:n.9529+3049del