Canonical Allele Identifier: CA775127637
Gene: SHBG HGNC NCBI

Linked Data

dbSNP Id: rs1461824370
gnomAD v3: 17-7618572-G-T
gnomAD v4: 17-7618572-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618572G>T , CM000679.2:g.7618572G>T GRCh38
NC_000017.10:g.7521890G>T , CM000679.1:g.7521890G>T GRCh37
NC_000017.9:g.7462615G>T NCBI36
NG_011981.2:g.9509G>T
NG_028105.1:g.1326C>A , LRG_285:g.1326C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4461G>T ENSP00000458875.1:n.-62+4461G>T
ENST00000572182.5:c.-62+4461G>T ENSP00000458816.1:n.-62+4461G>T
ENST00000572262.5:c.-62+4461G>T ENSP00000459999.1:n.-62+4461G>T
ENST00000574539.5:c.-62+4461G>T ENSP00000458181.1:n.-62+4461G>T
ENST00000575314.5:c.-62+4461G>T ENSP00000458559.1:n.-62+4461G>T
ENST00000576478.5:c.-62+4461G>T ENSP00000461133.1:n.-62+4461G>T
ENST00000576728.5:c.-62+4461G>T ENSP00000459620.1:n.-62+4461G>T
NM_001289114.1:c.-62+4461G>T NP_001276043.1:n.-62+4461G>T
NM_001289114.2:c.-62+4461G>T NP_001276043.1:n.-62+4461G>T