Canonical Allele Identifier: CA760016594
Gene:

Linked Data

dbSNP Id: rs1237922273

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458134del , CM000664.2:g.16458134del GRCh38
NC_000002.11:g.16639402del , CM000664.1:g.16639402del GRCh37
NC_000002.10:g.16502883del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3036del