Canonical Allele Identifier: CA537204532
Gene:

Linked Data

dbSNP Id: rs1200242635

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870650_155870653del , CM000664.2:g.155870650_155870653del GRCh38
NC_000002.11:g.156727162_156727165del , CM000664.1:g.156727162_156727165del GRCh37
NC_000002.10:g.156435408_156435411del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3466_320-3463del
XR_001739749.1:n.331-29669_331-29666del
XR_001739750.1:n.331-29669_331-29666del
XR_001739751.1:n.331-29669_331-29666del
XR_923501.2:n.331-3466_331-3463del