Canonical Allele Identifier: CA1457434234
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038298G= , CM000666.2:g.52038298G= GRCh38
NC_000004.11:g.52904464G= , CM000666.1:g.52904464G= GRCh37
NC_000004.10:g.52599221G= NCBI36
NG_008891.1:g.5022C= , LRG_204:g.5022C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-39C= MANE Select ENSP00000370839.6:n.-39C=
ENST00000381431.9:c.-39C= ENSP00000370839.5:n.-39C=
NM_000232.4:c.-39C= , LRG_204t1:c.-39C= NP_000223.1:n.-39C=
XM_011534403.1:c.-39C= XP_011532705.1:n.-39C=
NM_000232.5:c.-39C= MANE Select NP_000223.1:n.-39C=