Canonical Allele Identifier: CA2176996471

Gene: SCG3

Linked Data

• dbSNP Id: rs2055198471

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.51682091C>T , CM000677.2:g.51682091C>T	GRCh38
NC_000015.9:g.51974288C>T , CM000677.1:g.51974288C>T	GRCh37
NC_000015.8:g.49761580C>T	NCBI36
NG_013214.1:g.5739C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000220478.8:c.82+254C>T MANE Select	ENSP00000220478.3:n.82+254C>T
ENST00000220478.7:c.82+254C>T	ENSP00000220478.3:n.82+254C>T
ENST00000542355.6:c.-562+254C>T	ENSP00000445205.2:n.-562+254C>T
ENST00000558709.1:c.-419+254C>T	ENSP00000452745.1:n.-419+254C>T
NM_001165257.1:c.-562+254C>T	NP_001158729.1:n.-562+254C>T
NM_013243.3:c.82+254C>T	NP_037375.2:n.82+254C>T
NM_013243.4:c.82+254C>T MANE Select	NP_037375.2:n.82+254C>T
NM_001165257.2:c.-562+254C>T	NP_001158729.1:n.-562+254C>T