Canonical Allele Identifier: CA1457429108
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027963C= , CM000666.2:g.52027963C= GRCh38
NC_000004.11:g.52894129C= , CM000666.1:g.52894129C= GRCh37
NC_000004.10:g.52588886C= NCBI36
NG_008891.1:g.15357G= , LRG_204:g.15357G=

Transcript Alleles

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