Canonical Allele Identifier: CA535641068
Gene:

Linked Data

dbSNP Id: rs1347100092

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.127431658_127431660del , CM000664.2:g.127431658_127431660del GRCh38
NC_000002.11:g.128189234_128189236del , CM000664.1:g.128189234_128189236del GRCh37
NC_000002.10:g.127905704_127905706del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923313.1:n.1331+7_1331+9del
XR_001739705.1:n.3607-3396_3607-3394del
XR_923313.2:n.4042+7_4042+9del