Canonical Allele Identifier: CA2739265883
Gene: SGCB HGNC NCBI

Linked Data

ClinVar Variation Id: 2911544
ClinVar RCV Id: RCV003620358

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027948G>A , CM000666.2:g.52027948G>A GRCh38
NC_000004.11:g.52894114G>A , CM000666.1:g.52894114G>A GRCh37
NC_000004.10:g.52588871G>A NCBI36
NG_008891.1:g.15372C>T , LRG_204:g.15372C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+20C>T MANE Select ENSP00000370839.6:n.753+20C>T
ENST00000381431.9:c.753+20C>T ENSP00000370839.5:n.753+20C>T
NM_000232.4:c.753+20C>T , LRG_204t1:c.753+20C>T NP_000223.1:n.753+20C>T
XM_006714049.2:c.456+20C>T XP_006714112.1:n.456+20C>T
XM_011534403.1:c.543+20C>T XP_011532705.1:n.543+20C>T
XM_011534404.1:c.456+20C>T XP_011532706.1:n.456+20C>T
NM_000232.5:c.753+20C>T MANE Select NP_000223.1:n.753+20C>T