Canonical Allele Identifier: CA713642669

Gene: SCG3

Linked Data

• dbSNP Id: rs1296634536
• gnomAD v3: 15-51682044-G-A
• gnomAD v4: 15-51682044-G-A
• MyVariant Identifiers: chr15:g.51974241G>A (hg19) ; chr15:g.51682044G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51682044G>A , CM000677.2:g.51682044G>A	GRCh38
NC_000015.9:g.51974241G>A , CM000677.1:g.51974241G>A	GRCh37
NC_000015.8:g.49761533G>A	NCBI36
NG_013214.1:g.5692G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220478.8:c.82+207G>A MANE Select	ENSP00000220478.3:n.82+207G>A
ENST00000220478.7:c.82+207G>A	ENSP00000220478.3:n.82+207G>A
ENST00000542355.6:c.-562+207G>A	ENSP00000445205.2:n.-562+207G>A
ENST00000558709.1:c.-419+207G>A	ENSP00000452745.1:n.-419+207G>A
NM_001165257.1:c.-562+207G>A	NP_001158729.1:n.-562+207G>A
NM_013243.3:c.82+207G>A	NP_037375.2:n.82+207G>A
NM_013243.4:c.82+207G>A MANE Select	NP_037375.2:n.82+207G>A
NM_001165257.2:c.-562+207G>A	NP_001158729.1:n.-562+207G>A