Canonical Allele Identifier: CA2245918602
Gene: SHBG HGNC NCBI

Linked Data

dbSNP Id: rs2072031200
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618443_7618449del , CM000679.2:g.7618443_7618449del GRCh38
NC_000017.10:g.7521761_7521767del , CM000679.1:g.7521761_7521767del GRCh37
NC_000017.9:g.7462486_7462492del NCBI36
NG_011981.2:g.9380_9386del
NG_028105.1:g.1452_1458del , LRG_285:g.1452_1458del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4332_-62+4338del ENSP00000458875.1:n.-62+4332_-62+4338del
ENST00000572182.5:c.-62+4332_-62+4338del ENSP00000458816.1:n.-62+4332_-62+4338del
ENST00000572262.5:c.-62+4332_-62+4338del ENSP00000459999.1:n.-62+4332_-62+4338del
ENST00000574539.5:c.-62+4332_-62+4338del ENSP00000458181.1:n.-62+4332_-62+4338del
ENST00000575314.5:c.-62+4332_-62+4338del ENSP00000458559.1:n.-62+4332_-62+4338del
ENST00000576478.5:c.-62+4332_-62+4338del ENSP00000461133.1:n.-62+4332_-62+4338del
ENST00000576728.5:c.-62+4332_-62+4338del ENSP00000459620.1:n.-62+4332_-62+4338del
NM_001289114.1:c.-62+4332_-62+4338del NP_001276043.1:n.-62+4332_-62+4338del
NM_001289114.2:c.-62+4332_-62+4338del NP_001276043.1:n.-62+4332_-62+4338del
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