Canonical Allele Identifier: CA397894412

Gene: SHBG

Linked Data

• MyVariant Identifiers: chr17:g.7534680G>T (hg19) ; chr17:g.7631362G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7631362G>T , CM000679.2:g.7631362G>T	GRCh38
NC_000017.10:g.7534680G>T , CM000679.1:g.7534680G>T	GRCh37
NC_000017.9:g.7475405G>T	NCBI36
NG_011981.2:g.22299G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000380450.9:c.555+1G>T MANE Select	ENSP00000369816.4:n.555+1G>T
ENST00000340624.9:c.381+1G>T	ENSP00000345675.6:n.381+1G>T
ENST00000380450.8:c.555+1G>T	ENSP00000369816.4:n.555+1G>T
ENST00000416273.7:c.555+1G>T	ENSP00000388867.3:n.555+1G>T
ENST00000441599.6:c.555+1G>T	ENSP00000393426.2:n.555+1G>T
ENST00000570353.5:c.463+1G>T	ENSP00000458199.1:n.463+1G>T
ENST00000570527.5:c.*513+1G>T	ENSP00000461162.1:n.*513+1G>T
ENST00000570547.5:c.381+1G>T	ENSP00000458875.1:n.381+1G>T
ENST00000571153.5:c.313-227G>T	ENSP00000458858.1:n.313-227G>T
ENST00000572182.5:c.219+493G>T	ENSP00000458816.1:n.219+493G>T
ENST00000572262.5:c.220-227G>T	ENSP00000459999.1:n.220-227G>T
ENST00000574539.5:c.381+1G>T	ENSP00000458181.1:n.381+1G>T
ENST00000575314.5:c.381+1G>T	ENSP00000458559.1:n.381+1G>T
ENST00000575618.5:c.312+493G>T	ENSP00000459826.1:n.312+493G>T
ENST00000575903.5:c.555+1G>T	ENSP00000458973.1:n.555+1G>T
ENST00000576152.1:c.313-227G>T	ENSP00000461743.1:n.313-227G>T
ENST00000576478.5:c.220-227G>T	ENSP00000461133.1:n.220-227G>T
ENST00000576728.5:c.220-227G>T	ENSP00000459620.1:n.220-227G>T
ENST00000576747.1:n.53+1G>T
ENST00000576830.5:c.474+1G>T	ENSP00000460219.1:n.474+1G>T
NM_001040.4:c.555+1G>T	NP_001031.2:n.555+1G>T
NM_001146279.2:c.555+1G>T	NP_001139751.1:n.555+1G>T
NM_001146280.2:c.555+1G>T	NP_001139752.1:n.555+1G>T
NM_001146281.2:c.555+1G>T	NP_001139753.1:n.555+1G>T
NM_001289113.1:c.381+1G>T	NP_001276042.1:n.381+1G>T
NM_001289114.1:c.381+1G>T	NP_001276043.1:n.381+1G>T
NM_001289115.1:c.381+1G>T	NP_001276044.1:n.381+1G>T
NM_001289116.1:c.207+1G>T	NP_001276045.1:n.207+1G>T
XM_011523991.1:c.555+1G>T	XP_011522293.1:n.555+1G>T
NM_001040.5:c.555+1G>T MANE Select	NP_001031.2:n.555+1G>T
NM_001146279.3:c.555+1G>T	NP_001139751.1:n.555+1G>T
NM_001146280.3:c.555+1G>T	NP_001139752.1:n.555+1G>T
NM_001289116.2:c.207+1G>T	NP_001276045.1:n.207+1G>T
NM_001146281.3:c.555+1G>T	NP_001139753.1:n.555+1G>T
NM_001289113.2:c.381+1G>T	NP_001276042.1:n.381+1G>T
NM_001289114.2:c.381+1G>T	NP_001276043.1:n.381+1G>T
NM_001289115.2:c.381+1G>T	NP_001276044.1:n.381+1G>T