Canonical Allele Identifier: CA1300258793
Gene:

Linked Data

dbSNP Id: rs1683148547

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870595del , CM000664.2:g.155870595del GRCh38
NC_000002.11:g.156727107del , CM000664.1:g.156727107del GRCh37
NC_000002.10:g.156435353del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3408del
XR_001739749.1:n.331-29611del
XR_001739750.1:n.331-29611del
XR_001739751.1:n.331-29611del
XR_923501.2:n.331-3408del