Canonical Allele Identifier: CA775127576

Gene: SHBG

Linked Data

• dbSNP Id: rs1303481546
• MyVariant Identifiers: chr17:g.7521762_7521779del (hg19) ; chr17:g.7618444_7618461del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7618446_7618463del , CM000679.2:g.7618446_7618463del	GRCh38
NC_000017.10:g.7521764_7521781del , CM000679.1:g.7521764_7521781del	GRCh37
NC_000017.9:g.7462489_7462506del	NCBI36
NG_011981.2:g.9383_9400del
NG_028105.1:g.1437_1454del , LRG_285:g.1437_1454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570547.5:c.-62+4335_-62+4352del	ENSP00000458875.1:n.-62+4335_-62+4352del
ENST00000572182.5:c.-62+4335_-62+4352del	ENSP00000458816.1:n.-62+4335_-62+4352del
ENST00000572262.5:c.-62+4335_-62+4352del	ENSP00000459999.1:n.-62+4335_-62+4352del
ENST00000574539.5:c.-62+4335_-62+4352del	ENSP00000458181.1:n.-62+4335_-62+4352del
ENST00000575314.5:c.-62+4335_-62+4352del	ENSP00000458559.1:n.-62+4335_-62+4352del
ENST00000576478.5:c.-62+4335_-62+4352del	ENSP00000461133.1:n.-62+4335_-62+4352del
ENST00000576728.5:c.-62+4335_-62+4352del	ENSP00000459620.1:n.-62+4335_-62+4352del
NM_001289114.1:c.-62+4335_-62+4352del	NP_001276043.1:n.-62+4335_-62+4352del
NM_001289114.2:c.-62+4335_-62+4352del	NP_001276043.1:n.-62+4335_-62+4352del