Canonical Allele Identifier: CA1087465278
Gene:

Linked Data

dbSNP Id: rs1761786898

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31439975_31439983del , CM000668.2:g.31439975_31439983del GRCh38
NC_000006.11:g.31407752_31407760del , CM000668.1:g.31407752_31407760del GRCh37
NC_000006.10:g.31515731_31515739del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_926694.1:n.126_134del