Canonical Allele Identifier: CA2245918823

Gene: SHBG

Linked Data

• dbSNP Id: rs2072038024

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7618769_7618773dup , CM000679.2:g.7618769_7618773dup	GRCh38
NC_000017.10:g.7522087_7522091dup , CM000679.1:g.7522087_7522091dup	GRCh37
NC_000017.9:g.7462812_7462816dup	NCBI36
NG_011981.2:g.9706_9710dup
NG_028105.1:g.1125_1129dup , LRG_285:g.1125_1129dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570547.5:c.-62+4658_-62+4662dup	ENSP00000458875.1:n.-62+4658_-62+4662dup
ENST00000572182.5:c.-62+4658_-62+4662dup	ENSP00000458816.1:n.-62+4658_-62+4662dup
ENST00000572262.5:c.-62+4658_-62+4662dup	ENSP00000459999.1:n.-62+4658_-62+4662dup
ENST00000574539.5:c.-62+4658_-62+4662dup	ENSP00000458181.1:n.-62+4658_-62+4662dup
ENST00000575314.5:c.-62+4658_-62+4662dup	ENSP00000458559.1:n.-62+4658_-62+4662dup
ENST00000576478.5:c.-62+4658_-62+4662dup	ENSP00000461133.1:n.-62+4658_-62+4662dup
ENST00000576728.5:c.-62+4658_-62+4662dup	ENSP00000459620.1:n.-62+4658_-62+4662dup
NM_001289114.1:c.-62+4658_-62+4662dup	NP_001276043.1:n.-62+4658_-62+4662dup
NM_001289114.2:c.-62+4658_-62+4662dup	NP_001276043.1:n.-62+4658_-62+4662dup