Canonical Allele Identifier: CA617996995
Gene: SCG3 HGNC NCBI

Linked Data

dbSNP Id: rs200868173
gnomAD v2: 15-51974199-A-AT
gnomAD v3: 15-51682002-A-AT
gnomAD v4: 15-51682002-A-AT
MyVariant Identifiers: chr15:g.51974200_51974201insT (hg19) chr15:g.51974199_51974200insT (hg19) chr15:g.51682003_51682004insT (hg38) chr15:g.51682002_51682003insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51682010dup , CM000677.2:g.51682010dup GRCh38
NC_000015.9:g.51974207dup , CM000677.1:g.51974207dup GRCh37
NC_000015.8:g.49761499dup NCBI36
NG_013214.1:g.5658dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000220478.8:c.82+173dup MANE Select ENSP00000220478.3:n.82+173dup
ENST00000220478.7:c.82+173dup ENSP00000220478.3:n.82+173dup
ENST00000542355.6:c.-562+173dup ENSP00000445205.2:n.-562+173dup
ENST00000558709.1:c.-419+173dup ENSP00000452745.1:n.-419+173dup
NM_001165257.1:c.-562+173dup NP_001158729.1:n.-562+173dup
NM_013243.3:c.82+173dup NP_037375.2:n.82+173dup
NM_013243.4:c.82+173dup MANE Select NP_037375.2:n.82+173dup
NM_001165257.2:c.-562+173dup NP_001158729.1:n.-562+173dup
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