Canonical Allele Identifier: CA1121377258
Gene:

Linked Data

dbSNP Id: rs1824908775

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.12108907_12108916del , CM000671.2:g.12108907_12108916del GRCh38
NC_000009.11:g.12108907_12108916del , CM000671.1:g.12108907_12108916del GRCh37
NC_000009.10:g.12098907_12098916del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929481.1:n.166+7905_166+7914del
XR_929482.1:n.260+7905_260+7914del
XR_929481.2:n.166+7905_166+7914del
XR_929482.2:n.260+7905_260+7914del