Canonical Allele Identifier: CA59107088
Gene:

Linked Data

dbSNP Id: rs768314771

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870622_155870623del , CM000664.2:g.155870622_155870623del GRCh38
NC_000002.11:g.156727134_156727135del , CM000664.1:g.156727134_156727135del GRCh37
NC_000002.10:g.156435380_156435381del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3435_320-3434del
XR_001739749.1:n.331-29638_331-29637del
XR_001739750.1:n.331-29638_331-29637del
XR_001739751.1:n.331-29638_331-29637del
XR_923501.2:n.331-3435_331-3434del