Canonical Allele Identifier: CA2628476334
Gene: SCG3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51681927T>C , CM000677.2:g.51681927T>C GRCh38
NC_000015.9:g.51974124T>C , CM000677.1:g.51974124T>C GRCh37
NC_000015.8:g.49761416T>C NCBI36
NG_013214.1:g.5575T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000220478.8:c.82+90T>C MANE Select ENSP00000220478.3:n.82+90T>C
ENST00000220478.7:c.82+90T>C ENSP00000220478.3:n.82+90T>C
ENST00000542355.6:c.-562+90T>C ENSP00000445205.2:n.-562+90T>C
ENST00000558709.1:c.-419+90T>C ENSP00000452745.1:n.-419+90T>C
NM_001165257.1:c.-562+90T>C NP_001158729.1:n.-562+90T>C
NM_013243.3:c.82+90T>C NP_037375.2:n.82+90T>C
NM_013243.4:c.82+90T>C MANE Select NP_037375.2:n.82+90T>C
NM_001165257.2:c.-562+90T>C NP_001158729.1:n.-562+90T>C