Canonical Allele Identifier: CA14394715
Gene: SHBG HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12150660

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618597G>T , CM000679.2:g.7618597G>T GRCh38
NC_000017.10:g.7521915G>T , CM000679.1:g.7521915G>T GRCh37
NC_000017.9:g.7462640G>T NCBI36
NG_011981.2:g.9534G>T
NG_028105.1:g.1301C>A , LRG_285:g.1301C>A

Transcript Alleles

HGVS Amino-acid change
NM_001289114.1:c.-62+4486G>T VV NP_001276043.1:p.=
ENST00000570547.5:c.-62+4486G>T ENSP00000458875.1:p.=
ENST00000572182.5:c.-62+4486G>T ENSP00000458816.1:p.=
ENST00000572262.5:c.-62+4486G>T ENSP00000459999.1:p.=
ENST00000574539.5:c.-62+4486G>T ENSP00000458181.1:p.=
ENST00000575314.5:c.-62+4486G>T ENSP00000458559.1:p.=
ENST00000576478.5:c.-62+4486G>T ENSP00000461133.1:p.=
ENST00000576728.5:c.-62+4486G>T ENSP00000459620.1:p.=