Canonical Allele Identifier: CA2635889255

Gene: SHBG

Linked Data

• gnomAD v4: 17-7630297-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7630297A>G , CM000679.2:g.7630297A>G	GRCh38
NC_000017.10:g.7533615A>G , CM000679.1:g.7533615A>G	GRCh37
NC_000017.9:g.7474340A>G	NCBI36
NG_011981.2:g.21234A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380450.9:c.111+14A>G MANE Select	ENSP00000369816.4:n.111+14A>G
ENST00000340624.9:c.-63-119A>G	ENSP00000345675.6:n.-63-119A>G
ENST00000380450.8:c.111+14A>G	ENSP00000369816.4:n.111+14A>G
ENST00000416273.7:c.111+14A>G	ENSP00000388867.3:n.111+14A>G
ENST00000441599.6:c.111+14A>G	ENSP00000393426.2:n.111+14A>G
ENST00000570353.5:c.111+14A>G	ENSP00000458199.1:n.111+14A>G
ENST00000570527.5:c.125A>G	ENSP00000461162.1:p.Asp42Gly
ENST00000570547.5:c.-61-121A>G	ENSP00000458875.1:n.-61-121A>G
ENST00000571153.5:c.30+14A>G	ENSP00000458858.1:n.30+14A>G
ENST00000572182.5:c.-61-121A>G	ENSP00000458816.1:n.-61-121A>G
ENST00000572262.5:c.-61-121A>G	ENSP00000459999.1:n.-61-121A>G
ENST00000574539.5:c.-61-121A>G	ENSP00000458181.1:n.-61-121A>G
ENST00000575314.5:c.-61-121A>G	ENSP00000458559.1:n.-61-121A>G
ENST00000575618.5:c.30+14A>G	ENSP00000459826.1:n.30+14A>G
ENST00000575729.5:c.-63-119A>G	ENSP00000458719.1:n.-63-119A>G
ENST00000575903.5:c.111+14A>G	ENSP00000458973.1:n.111+14A>G
ENST00000576152.1:c.30+14A>G	ENSP00000461743.1:n.30+14A>G
ENST00000576478.5:c.-61-121A>G	ENSP00000461133.1:n.-61-121A>G
ENST00000576728.5:c.-61-121A>G	ENSP00000459620.1:n.-61-121A>G
ENST00000576830.5:c.30+14A>G	ENSP00000460219.1:n.30+14A>G
NM_001040.4:c.111+14A>G	NP_001031.2:n.111+14A>G
NM_001146279.2:c.111+14A>G	NP_001139751.1:n.111+14A>G
NM_001146280.2:c.111+14A>G	NP_001139752.1:n.111+14A>G
NM_001146281.2:c.111+14A>G	NP_001139753.1:n.111+14A>G
NM_001289113.1:c.-63-119A>G	NP_001276042.1:n.-63-119A>G
NM_001289114.1:c.-61-121A>G	NP_001276043.1:n.-61-121A>G
NM_001289115.1:c.-63-119A>G	NP_001276044.1:n.-63-119A>G
NM_001289116.1:c.-146+14A>G	NP_001276045.1:n.-146+14A>G
XM_011523991.1:c.111+14A>G	XP_011522293.1:n.111+14A>G
NM_001040.5:c.111+14A>G MANE Select	NP_001031.2:n.111+14A>G
NM_001146279.3:c.111+14A>G	NP_001139751.1:n.111+14A>G
NM_001146280.3:c.111+14A>G	NP_001139752.1:n.111+14A>G
NM_001289116.2:c.-146+14A>G	NP_001276045.1:n.-146+14A>G
NM_001146281.3:c.111+14A>G	NP_001139753.1:n.111+14A>G
NM_001289113.2:c.-63-119A>G	NP_001276042.1:n.-63-119A>G
NM_001289114.2:c.-61-121A>G	NP_001276043.1:n.-61-121A>G
NM_001289115.2:c.-63-119A>G	NP_001276044.1:n.-63-119A>G