Canonical Allele Identifier: CA2245918614
Gene: SHBG HGNC NCBI

Linked Data

dbSNP Id: rs2072031602

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618446_7618457del , CM000679.2:g.7618446_7618457del GRCh38
NC_000017.10:g.7521764_7521775del , CM000679.1:g.7521764_7521775del GRCh37
NC_000017.9:g.7462489_7462500del NCBI36
NG_011981.2:g.9383_9394del
NG_028105.1:g.1443_1454del , LRG_285:g.1443_1454del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4335_-62+4346del ENSP00000458875.1:n.-62+4335_-62+4346del
ENST00000572182.5:c.-62+4335_-62+4346del ENSP00000458816.1:n.-62+4335_-62+4346del
ENST00000572262.5:c.-62+4335_-62+4346del ENSP00000459999.1:n.-62+4335_-62+4346del
ENST00000574539.5:c.-62+4335_-62+4346del ENSP00000458181.1:n.-62+4335_-62+4346del
ENST00000575314.5:c.-62+4335_-62+4346del ENSP00000458559.1:n.-62+4335_-62+4346del
ENST00000576478.5:c.-62+4335_-62+4346del ENSP00000461133.1:n.-62+4335_-62+4346del
ENST00000576728.5:c.-62+4335_-62+4346del ENSP00000459620.1:n.-62+4335_-62+4346del
NM_001289114.1:c.-62+4335_-62+4346del NP_001276043.1:n.-62+4335_-62+4346del
NM_001289114.2:c.-62+4335_-62+4346del NP_001276043.1:n.-62+4335_-62+4346del