Canonical Allele Identifier: CA287485303

Gene: SHBG

Linked Data

• dbSNP Id: rs995240210
• gnomAD v3: 17-7618587-A-G
• gnomAD v4: 17-7618587-A-G
• MyVariant Identifiers: chr17:g.7521905A>G (hg19) ; chr17:g.7618587A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7618587A>G , CM000679.2:g.7618587A>G	GRCh38
NC_000017.10:g.7521905A>G , CM000679.1:g.7521905A>G	GRCh37
NC_000017.9:g.7462630A>G	NCBI36
NG_011981.2:g.9524A>G
NG_028105.1:g.1311T>C , LRG_285:g.1311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570547.5:c.-62+4476A>G	ENSP00000458875.1:n.-62+4476A>G
ENST00000572182.5:c.-62+4476A>G	ENSP00000458816.1:n.-62+4476A>G
ENST00000572262.5:c.-62+4476A>G	ENSP00000459999.1:n.-62+4476A>G
ENST00000574539.5:c.-62+4476A>G	ENSP00000458181.1:n.-62+4476A>G
ENST00000575314.5:c.-62+4476A>G	ENSP00000458559.1:n.-62+4476A>G
ENST00000576478.5:c.-62+4476A>G	ENSP00000461133.1:n.-62+4476A>G
ENST00000576728.5:c.-62+4476A>G	ENSP00000459620.1:n.-62+4476A>G
NM_001289114.1:c.-62+4476A>G	NP_001276043.1:n.-62+4476A>G
NM_001289114.2:c.-62+4476A>G	NP_001276043.1:n.-62+4476A>G