Canonical Allele Identifier: CA2638110332
Gene: SOST HGNC NCBI

Linked Data

gnomAD v4: 17-43755854-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43755854G>T , CM000679.2:g.43755854G>T GRCh38
NC_000017.10:g.41833222G>T , CM000679.1:g.41833222G>T GRCh37
NC_000017.9:g.39188748G>T NCBI36
NG_008078.2:g.7935C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301691.3:c.221-91C>A MANE Select ENSP00000301691.1:n.221-91C>A
ENST00000301691.2:c.221-91C>A ENSP00000301691.1:n.221-91C>A
NM_025237.2:c.221-91C>A NP_079513.1:n.221-91C>A
NM_025237.3:c.221-91C>A MANE Select NP_079513.1:n.221-91C>A
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