Canonical Allele Identifier: CA2635888994

Gene: SHBG

Linked Data

• gnomAD v4: 17-7630133-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7630133C>G , CM000679.2:g.7630133C>G	GRCh38
NC_000017.10:g.7533451C>G , CM000679.1:g.7533451C>G	GRCh37
NC_000017.9:g.7474176C>G	NCBI36
NG_011981.2:g.21070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000340624.9:c.-63-283C>G	ENSP00000345675.6:n.-63-283C>G
ENST00000441599.6:c.-40C>G	ENSP00000393426.2:n.-40C>G
ENST00000570547.5:c.-61-285C>G	ENSP00000458875.1:n.-61-285C>G
ENST00000572182.5:c.-61-285C>G	ENSP00000458816.1:n.-61-285C>G
ENST00000572262.5:c.-61-285C>G	ENSP00000459999.1:n.-61-285C>G
ENST00000574539.5:c.-61-285C>G	ENSP00000458181.1:n.-61-285C>G
ENST00000575314.5:c.-61-285C>G	ENSP00000458559.1:n.-61-285C>G
ENST00000575729.5:c.-63-283C>G	ENSP00000458719.1:n.-63-283C>G
ENST00000576478.5:c.-61-285C>G	ENSP00000461133.1:n.-61-285C>G
ENST00000576728.5:c.-61-285C>G	ENSP00000459620.1:n.-61-285C>G
NM_001040.4:c.-40C>G	NP_001031.2:n.-40C>G
NM_001146279.2:c.-40C>G	NP_001139751.1:n.-40C>G
NM_001146280.2:c.-40C>G	NP_001139752.1:n.-40C>G
NM_001146281.2:c.-40C>G	NP_001139753.1:n.-40C>G
NM_001289113.1:c.-63-283C>G	NP_001276042.1:n.-63-283C>G
NM_001289114.1:c.-61-285C>G	NP_001276043.1:n.-61-285C>G
NM_001289115.1:c.-63-283C>G	NP_001276044.1:n.-63-283C>G
NM_001289116.1:c.-296C>G	NP_001276045.1:n.-296C>G
XM_011523991.1:c.-40C>G	XP_011522293.1:n.-40C>G
NM_001289113.2:c.-63-283C>G	NP_001276042.1:n.-63-283C>G
NM_001289114.2:c.-61-285C>G	NP_001276043.1:n.-61-285C>G
NM_001289115.2:c.-63-283C>G	NP_001276044.1:n.-63-283C>G