Canonical Allele Identifier: CA270568901

Gene: SCG3

Linked Data

• dbSNP Id: rs370730192
• gnomAD v2: 15-51974279-C-A
• gnomAD v3: 15-51682082-C-A
• gnomAD v4: 15-51682082-C-A
• MyVariant Identifiers: chr15:g.51974279C>A (hg19) ; chr15:g.51682082C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51682082C>A , CM000677.2:g.51682082C>A	GRCh38
NC_000015.9:g.51974279C>A , CM000677.1:g.51974279C>A	GRCh37
NC_000015.8:g.49761571C>A	NCBI36
NG_013214.1:g.5730C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220478.8:c.82+245C>A MANE Select	ENSP00000220478.3:n.82+245C>A
ENST00000220478.7:c.82+245C>A	ENSP00000220478.3:n.82+245C>A
ENST00000542355.6:c.-562+245C>A	ENSP00000445205.2:n.-562+245C>A
ENST00000558709.1:c.-419+245C>A	ENSP00000452745.1:n.-419+245C>A
NM_001165257.1:c.-562+245C>A	NP_001158729.1:n.-562+245C>A
NM_013243.3:c.82+245C>A	NP_037375.2:n.82+245C>A
NM_013243.4:c.82+245C>A MANE Select	NP_037375.2:n.82+245C>A
NM_001165257.2:c.-562+245C>A	NP_001158729.1:n.-562+245C>A