Canonical Allele Identifier: CA1457434205
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038266G= , CM000666.2:g.52038266G= GRCh38
NC_000004.11:g.52904432G= , CM000666.1:g.52904432G= GRCh37
NC_000004.10:g.52599189G= NCBI36
NG_008891.1:g.5054C= , LRG_204:g.5054C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-7C= MANE Select ENSP00000370839.6:n.-7C=
ENST00000381431.9:c.-7C= ENSP00000370839.5:n.-7C=
NM_000232.4:c.-7C= , LRG_204t1:c.-7C= NP_000223.1:n.-7C=
XM_011534403.1:c.-7C= XP_011532705.1:n.-7C=
NM_000232.5:c.-7C= MANE Select NP_000223.1:n.-7C=