Canonical Allele Identifier: CA1841175639
Gene:

Linked Data

dbSNP Id: rs1819678411

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551518del , CM000671.2:g.25551518del GRCh38
NC_000009.11:g.25551516del , CM000671.1:g.25551516del GRCh37
NC_000009.10:g.25541516del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-946del
XR_929525.2:n.674-946del