Canonical Allele Identifier: CA1035793691
Gene:

Linked Data

dbSNP Id: rs1678947439

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368908del , CM000664.2:g.122368908del GRCh38
NC_000002.11:g.123126484del , CM000664.1:g.123126484del GRCh37
NC_000002.10:g.122842954del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24055del
XR_001739684.1:n.556-24055del