Canonical Allele Identifier: CA919821901
Gene:

Linked Data

dbSNP Id: rs1555553619

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.29376286_29376287del , CM000679.2:g.29376286_29376287del GRCh38
NC_000017.10:g.27703304_27703305del , CM000679.1:g.27703304_27703305del GRCh37
NC_000017.9:g.24727430_24727431del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011525588.1:c.1008-5982_1008-5981del XP_011523890.1:n.1008-5982_1008-5981del