Canonical Allele Identifier: CA775127645
Gene: SHBG HGNC NCBI

Linked Data

dbSNP Id: rs1201945786
gnomAD v3: 17-7618585-GCATGAGC-G
gnomAD v4: 17-7618585-GCATGAGC-G
MyVariant Identifiers: chr17:g.7521904_7521910del (hg19) chr17:g.7618586_7618592del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7618588_7618594del , CM000679.2:g.7618588_7618594del GRCh38
NC_000017.10:g.7521906_7521912del , CM000679.1:g.7521906_7521912del GRCh37
NC_000017.9:g.7462631_7462637del NCBI36
NG_011981.2:g.9525_9531del
NG_028105.1:g.1306_1312del , LRG_285:g.1306_1312del

Transcript Alleles

HGVS Amino-acid Change
ENST00000570547.5:c.-62+4477_-62+4483del ENSP00000458875.1:n.-62+4477_-62+4483del
ENST00000572182.5:c.-62+4477_-62+4483del ENSP00000458816.1:n.-62+4477_-62+4483del
ENST00000572262.5:c.-62+4477_-62+4483del ENSP00000459999.1:n.-62+4477_-62+4483del
ENST00000574539.5:c.-62+4477_-62+4483del ENSP00000458181.1:n.-62+4477_-62+4483del
ENST00000575314.5:c.-62+4477_-62+4483del ENSP00000458559.1:n.-62+4477_-62+4483del
ENST00000576478.5:c.-62+4477_-62+4483del ENSP00000461133.1:n.-62+4477_-62+4483del
ENST00000576728.5:c.-62+4477_-62+4483del ENSP00000459620.1:n.-62+4477_-62+4483del
NM_001289114.1:c.-62+4477_-62+4483del NP_001276043.1:n.-62+4477_-62+4483del
NM_001289114.2:c.-62+4477_-62+4483del NP_001276043.1:n.-62+4477_-62+4483del
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