Canonical Allele Identifier: CA2072411552
Gene:

Linked Data

dbSNP Id: rs1953653260

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.131529696_131529700del , CM000674.2:g.131529696_131529700del GRCh38
NC_000012.11:g.132014241_132014245del , CM000674.1:g.132014241_132014245del GRCh37
NC_000012.10:g.130580194_130580198del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945564.1:n.1076+75_1076+79del
XR_001749407.2:n.1067+75_1067+79del