Canonical Allele Identifier: CA1457429062
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027861A= , CM000666.2:g.52027861A= GRCh38
NC_000004.11:g.52894027A= , CM000666.1:g.52894027A= GRCh37
NC_000004.10:g.52588784A= NCBI36
NG_008891.1:g.15459T= , LRG_204:g.15459T=

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+107T= MANE Select ENSP00000370839.6:n.753+107T=
ENST00000381431.9:c.753+107T= ENSP00000370839.5:n.753+107T=
NM_000232.4:c.753+107T= , LRG_204t1:c.753+107T= NP_000223.1:n.753+107T=
XM_006714049.2:c.456+107T= XP_006714112.1:n.456+107T=
XM_011534403.1:c.543+107T= XP_011532705.1:n.543+107T=
XM_011534404.1:c.456+107T= XP_011532706.1:n.456+107T=
NM_000232.5:c.753+107T= MANE Select NP_000223.1:n.753+107T=