Canonical Allele Identifier: CA1457434337
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038429T= , CM000666.2:g.52038429T= GRCh38
NC_000004.11:g.52904595T= , CM000666.1:g.52904595T= GRCh37
NC_000004.10:g.52599352T= NCBI36
NG_008891.1:g.4891A= , LRG_204:g.4891A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-170A= ENSP00000370839.5:n.-170A=