Canonical Allele Identifier: CA2670614721
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038302-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038302C>A , CM000666.2:g.52038302C>A GRCh38
NC_000004.11:g.52904468C>A , CM000666.1:g.52904468C>A GRCh37
NC_000004.10:g.52599225C>A NCBI36
NG_008891.1:g.5018G>T , LRG_204:g.5018G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-43G>T ENSP00000370839.5:n.-43G>T
NM_000232.4:c.-43G>T , LRG_204t1:c.-43G>T NP_000223.1:n.-43G>T