Canonical Allele Identifier: CA59107059
Gene:

Linked Data

dbSNP Id: rs769622503

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870353_155870354del , CM000664.2:g.155870353_155870354del GRCh38
NC_000002.11:g.156726865_156726866del , CM000664.1:g.156726865_156726866del GRCh37
NC_000002.10:g.156435111_156435112del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3165_320-3164del
XR_001739749.1:n.331-29368_331-29367del
XR_001739750.1:n.331-29368_331-29367del
XR_001739751.1:n.331-29368_331-29367del
XR_923501.2:n.331-3165_331-3164del