Canonical Allele Identifier: CA2176996476
Gene: SCG3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.51682093T= , CM000677.2:g.51682093T= GRCh38
NC_000015.9:g.51974290T= , CM000677.1:g.51974290T= GRCh37
NC_000015.8:g.49761582T= NCBI36
NG_013214.1:g.5741T=

Transcript Alleles

HGVS Amino-acid change
ENST00000220478.8:c.82+256T= MANE Select ENSP00000220478.3:n.82+256T=
ENST00000220478.7:c.82+256T= ENSP00000220478.3:n.82+256T=
ENST00000542355.6:c.-562+256T= ENSP00000445205.2:n.-562+256T=
ENST00000558709.1:c.-419+256T= ENSP00000452745.1:n.-419+256T=
NM_001165257.1:c.-562+256T= NP_001158729.1:n.-562+256T=
NM_013243.3:c.82+256T= NP_037375.2:n.82+256T=
NM_013243.4:c.82+256T= MANE Select NP_037375.2:n.82+256T=
NM_001165257.2:c.-562+256T= NP_001158729.1:n.-562+256T=