Canonical Allele Identifier: CA2245918632
Gene: SHBG HGNC NCBI

Linked Data

dbSNP Id: rs2072032175

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618455_7618469dup , CM000679.2:g.7618455_7618469dup GRCh38
NC_000017.10:g.7521773_7521787dup , CM000679.1:g.7521773_7521787dup GRCh37
NC_000017.9:g.7462498_7462512dup NCBI36
NG_011981.2:g.9392_9406dup
NG_028105.1:g.1431_1445dup , LRG_285:g.1431_1445dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4344_-62+4358dup ENSP00000458875.1:n.-62+4344_-62+4358dup
ENST00000572182.5:c.-62+4344_-62+4358dup ENSP00000458816.1:n.-62+4344_-62+4358dup
ENST00000572262.5:c.-62+4344_-62+4358dup ENSP00000459999.1:n.-62+4344_-62+4358dup
ENST00000574539.5:c.-62+4344_-62+4358dup ENSP00000458181.1:n.-62+4344_-62+4358dup
ENST00000575314.5:c.-62+4344_-62+4358dup ENSP00000458559.1:n.-62+4344_-62+4358dup
ENST00000576478.5:c.-62+4344_-62+4358dup ENSP00000461133.1:n.-62+4344_-62+4358dup
ENST00000576728.5:c.-62+4344_-62+4358dup ENSP00000459620.1:n.-62+4344_-62+4358dup
NM_001289114.1:c.-62+4344_-62+4358dup NP_001276043.1:n.-62+4344_-62+4358dup
NM_001289114.2:c.-62+4344_-62+4358dup NP_001276043.1:n.-62+4344_-62+4358dup