Canonical Allele Identifier: CA287485339

Gene: SHBG

Linked Data

• dbSNP Id: rs544922304
• MyVariant Identifiers: chr17:g.7522048G>C (hg19) ; chr17:g.7618730G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7618730G>C , CM000679.2:g.7618730G>C	GRCh38
NC_000017.10:g.7522048G>C , CM000679.1:g.7522048G>C	GRCh37
NC_000017.9:g.7462773G>C	NCBI36
NG_011981.2:g.9667G>C
NG_028105.1:g.1168C>G , LRG_285:g.1168C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000570547.5:c.-62+4619G>C	ENSP00000458875.1:n.-62+4619G>C
ENST00000572182.5:c.-62+4619G>C	ENSP00000458816.1:n.-62+4619G>C
ENST00000572262.5:c.-62+4619G>C	ENSP00000459999.1:n.-62+4619G>C
ENST00000574539.5:c.-62+4619G>C	ENSP00000458181.1:n.-62+4619G>C
ENST00000575314.5:c.-62+4619G>C	ENSP00000458559.1:n.-62+4619G>C
ENST00000576478.5:c.-62+4619G>C	ENSP00000461133.1:n.-62+4619G>C
ENST00000576728.5:c.-62+4619G>C	ENSP00000459620.1:n.-62+4619G>C
NM_001289114.1:c.-62+4619G>C	NP_001276043.1:n.-62+4619G>C
NM_001289114.2:c.-62+4619G>C	NP_001276043.1:n.-62+4619G>C