Canonical Allele Identifier: CA713642695

Gene: SCG3

Linked Data

• dbSNP Id: rs1338526332
• gnomAD v3: 15-51682048-T-C
• gnomAD v4: 15-51682048-T-C
• MyVariant Identifiers: chr15:g.51974245T>C (hg19) ; chr15:g.51682048T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51682048T>C , CM000677.2:g.51682048T>C	GRCh38
NC_000015.9:g.51974245T>C , CM000677.1:g.51974245T>C	GRCh37
NC_000015.8:g.49761537T>C	NCBI36
NG_013214.1:g.5696T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000220478.8:c.82+211T>C MANE Select	ENSP00000220478.3:n.82+211T>C
ENST00000220478.7:c.82+211T>C	ENSP00000220478.3:n.82+211T>C
ENST00000542355.6:c.-562+211T>C	ENSP00000445205.2:n.-562+211T>C
ENST00000558709.1:c.-419+211T>C	ENSP00000452745.1:n.-419+211T>C
NM_001165257.1:c.-562+211T>C	NP_001158729.1:n.-562+211T>C
NM_013243.3:c.82+211T>C	NP_037375.2:n.82+211T>C
NM_013243.4:c.82+211T>C MANE Select	NP_037375.2:n.82+211T>C
NM_001165257.2:c.-562+211T>C	NP_001158729.1:n.-562+211T>C