Canonical Allele Identifier: CA1457434201
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038263C= , CM000666.2:g.52038263C= GRCh38
NC_000004.11:g.52904429C= , CM000666.1:g.52904429C= GRCh37
NC_000004.10:g.52599186C= NCBI36
NG_008891.1:g.5057G= , LRG_204:g.5057G=

Transcript Alleles

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