Canonical Allele Identifier: CA41586360
Gene:

Linked Data

dbSNP Id: rs1014779823

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.773294_773297del , CM000664.2:g.773294_773297del GRCh38
NC_000002.11:g.773294_773297del , CM000664.1:g.773294_773297del GRCh37
NC_000002.10:g.763294_763297del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011510439.1:c.-24-3542_-24-3539del XP_011508741.1:n.-24-3542_-24-3539del
XM_011510440.1:c.-24-3542_-24-3539del XP_011508742.1:n.-24-3542_-24-3539del
XM_011510441.1:c.-24-3542_-24-3539del XP_011508743.1:n.-24-3542_-24-3539del
XM_011510442.1:c.-24-3542_-24-3539del XP_011508744.1:n.-24-3542_-24-3539del
XM_011510443.1:c.-24-3542_-24-3539del XP_011508745.1:n.-24-3542_-24-3539del
XR_922708.1:n.4001-3542_4001-3539del