Canonical Allele Identifier: CA287485259

Gene: SHBG

Linked Data

• dbSNP Id: rs72829406
• gnomAD v2: 17-7521764-T-G
• gnomAD v3: 17-7618446-T-G
• gnomAD v4: 17-7618446-T-G
• MyVariant Identifiers: chr17:g.7521764T>G (hg19) ; chr17:g.7521764_7521776delinsGTTTTTGTTTTTG (hg19) ; chr17:g.7618446T>G (hg38) ; chr17:g.7618446_7618458delinsGTTTTTGTTTTTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7618446T>G , CM000679.2:g.7618446T>G	GRCh38
NC_000017.10:g.7521764T>G , CM000679.1:g.7521764T>G	GRCh37
NC_000017.9:g.7462489T>G	NCBI36
NG_011981.2:g.9383T>G
NG_028105.1:g.1452A>C , LRG_285:g.1452A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000570547.5:c.-62+4335T>G	ENSP00000458875.1:n.-62+4335T>G
ENST00000572182.5:c.-62+4335T>G	ENSP00000458816.1:n.-62+4335T>G
ENST00000572262.5:c.-62+4335T>G	ENSP00000459999.1:n.-62+4335T>G
ENST00000574539.5:c.-62+4335T>G	ENSP00000458181.1:n.-62+4335T>G
ENST00000575314.5:c.-62+4335T>G	ENSP00000458559.1:n.-62+4335T>G
ENST00000576478.5:c.-62+4335T>G	ENSP00000461133.1:n.-62+4335T>G
ENST00000576728.5:c.-62+4335T>G	ENSP00000459620.1:n.-62+4335T>G
NM_001289114.1:c.-62+4335T>G	NP_001276043.1:n.-62+4335T>G
NM_001289114.2:c.-62+4335T>G	NP_001276043.1:n.-62+4335T>G