Canonical Allele Identifier: CA2245918606
Gene: SHBG HGNC NCBI

Linked Data

dbSNP Id: rs2072031262
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618443G>A , CM000679.2:g.7618443G>A GRCh38
NC_000017.10:g.7521761G>A , CM000679.1:g.7521761G>A GRCh37
NC_000017.9:g.7462486G>A NCBI36
NG_011981.2:g.9380G>A
NG_028105.1:g.1455C>T , LRG_285:g.1455C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4332G>A ENSP00000458875.1:n.-62+4332G>A
ENST00000572182.5:c.-62+4332G>A ENSP00000458816.1:n.-62+4332G>A
ENST00000572262.5:c.-62+4332G>A ENSP00000459999.1:n.-62+4332G>A
ENST00000574539.5:c.-62+4332G>A ENSP00000458181.1:n.-62+4332G>A
ENST00000575314.5:c.-62+4332G>A ENSP00000458559.1:n.-62+4332G>A
ENST00000576478.5:c.-62+4332G>A ENSP00000461133.1:n.-62+4332G>A
ENST00000576728.5:c.-62+4332G>A ENSP00000459620.1:n.-62+4332G>A
NM_001289114.1:c.-62+4332G>A NP_001276043.1:n.-62+4332G>A
NM_001289114.2:c.-62+4332G>A NP_001276043.1:n.-62+4332G>A
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