Canonical Allele Identifier: CA2245927317
Gene: SHBG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7630041T= , CM000679.2:g.7630041T= GRCh38
NC_000017.10:g.7533359T= , CM000679.1:g.7533359T= GRCh37
NC_000017.9:g.7474084T= NCBI36
NG_011981.2:g.20978T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340624.9:c.-63-375T= ENSP00000345675.6:n.-63-375T=
ENST00000570547.5:c.-61-377T= ENSP00000458875.1:n.-61-377T=
ENST00000572182.5:c.-61-377T= ENSP00000458816.1:n.-61-377T=
ENST00000572262.5:c.-61-377T= ENSP00000459999.1:n.-61-377T=
ENST00000574539.5:c.-61-377T= ENSP00000458181.1:n.-61-377T=
ENST00000575314.5:c.-61-377T= ENSP00000458559.1:n.-61-377T=
ENST00000575729.5:c.-63-375T= ENSP00000458719.1:n.-63-375T=
ENST00000576478.5:c.-61-377T= ENSP00000461133.1:n.-61-377T=
ENST00000576728.5:c.-61-377T= ENSP00000459620.1:n.-61-377T=
NM_001289113.1:c.-63-375T= NP_001276042.1:n.-63-375T=
NM_001289114.1:c.-61-377T= NP_001276043.1:n.-61-377T=
NM_001289115.1:c.-63-375T= NP_001276044.1:n.-63-375T=
NM_001289113.2:c.-63-375T= NP_001276042.1:n.-63-375T=
NM_001289114.2:c.-61-377T= NP_001276043.1:n.-61-377T=
NM_001289115.2:c.-63-375T= NP_001276044.1:n.-63-375T=