Canonical Allele Identifier: CA2635888868

Gene: SHBG

Linked Data

• gnomAD v4: 17-7630020-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7630020C>T , CM000679.2:g.7630020C>T	GRCh38
NC_000017.10:g.7533338C>T , CM000679.1:g.7533338C>T	GRCh37
NC_000017.9:g.7474063C>T	NCBI36
NG_011981.2:g.20957C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000340624.9:c.-63-396C>T	ENSP00000345675.6:n.-63-396C>T
ENST00000570547.5:c.-61-398C>T	ENSP00000458875.1:n.-61-398C>T
ENST00000572182.5:c.-61-398C>T	ENSP00000458816.1:n.-61-398C>T
ENST00000572262.5:c.-61-398C>T	ENSP00000459999.1:n.-61-398C>T
ENST00000574539.5:c.-61-398C>T	ENSP00000458181.1:n.-61-398C>T
ENST00000575314.5:c.-61-398C>T	ENSP00000458559.1:n.-61-398C>T
ENST00000575729.5:c.-63-396C>T	ENSP00000458719.1:n.-63-396C>T
ENST00000576478.5:c.-61-398C>T	ENSP00000461133.1:n.-61-398C>T
ENST00000576728.5:c.-61-398C>T	ENSP00000459620.1:n.-61-398C>T
NM_001289113.1:c.-63-396C>T	NP_001276042.1:n.-63-396C>T
NM_001289114.1:c.-61-398C>T	NP_001276043.1:n.-61-398C>T
NM_001289115.1:c.-63-396C>T	NP_001276044.1:n.-63-396C>T
NM_001289113.2:c.-63-396C>T	NP_001276042.1:n.-63-396C>T
NM_001289114.2:c.-61-398C>T	NP_001276043.1:n.-61-398C>T
NM_001289115.2:c.-63-396C>T	NP_001276044.1:n.-63-396C>T