Canonical Allele Identifier: CA1247519059
Gene:

Linked Data

dbSNP Id: rs1667990379

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.41534566del , CM000664.2:g.41534566del GRCh38
NC_000002.11:g.41761706del , CM000664.1:g.41761706del GRCh37
NC_000002.10:g.41615210del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939996.1:n.181+3160del
XR_939997.1:n.146+3160del
XR_939997.2:n.9529+3160del