Canonical Allele Identifier: CA2638110260
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755793-C-CG
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755794dup , CM000679.2:g.43755794dup GRCh38
NC_000017.10:g.41833162dup , CM000679.1:g.41833162dup GRCh37
NC_000017.9:g.39188688dup NCBI36
NG_008078.2:g.7995dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-31dup MANE Select ENSP00000301691.1:n.221-31dup
ENST00000301691.2:c.221-31dup ENSP00000301691.1:n.221-31dup
NM_025237.2:c.221-31dup NP_079513.1:n.221-31dup
NM_025237.3:c.221-31dup MANE Select NP_079513.1:n.221-31dup
Search 100 bp 5'
Search 100 bp 3'