Canonical Allele Identifier: CA2245927312
Gene: SHBG HGNC NCBI

Linked Data

dbSNP Id: rs2072346236

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7630033G>A , CM000679.2:g.7630033G>A GRCh38
NC_000017.10:g.7533351G>A , CM000679.1:g.7533351G>A GRCh37
NC_000017.9:g.7474076G>A NCBI36
NG_011981.2:g.20970G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000340624.9:c.-63-383G>A ENSP00000345675.6:n.-63-383G>A
ENST00000570547.5:c.-61-385G>A ENSP00000458875.1:n.-61-385G>A
ENST00000572182.5:c.-61-385G>A ENSP00000458816.1:n.-61-385G>A
ENST00000572262.5:c.-61-385G>A ENSP00000459999.1:n.-61-385G>A
ENST00000574539.5:c.-61-385G>A ENSP00000458181.1:n.-61-385G>A
ENST00000575314.5:c.-61-385G>A ENSP00000458559.1:n.-61-385G>A
ENST00000575729.5:c.-63-383G>A ENSP00000458719.1:n.-63-383G>A
ENST00000576478.5:c.-61-385G>A ENSP00000461133.1:n.-61-385G>A
ENST00000576728.5:c.-61-385G>A ENSP00000459620.1:n.-61-385G>A
NM_001289113.1:c.-63-383G>A NP_001276042.1:n.-63-383G>A
NM_001289114.1:c.-61-385G>A NP_001276043.1:n.-61-385G>A
NM_001289115.1:c.-63-383G>A NP_001276044.1:n.-63-383G>A
NM_001289113.2:c.-63-383G>A NP_001276042.1:n.-63-383G>A
NM_001289114.2:c.-61-385G>A NP_001276043.1:n.-61-385G>A
NM_001289115.2:c.-63-383G>A NP_001276044.1:n.-63-383G>A