Canonical Allele Identifier: CA2670614801
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038345-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038345T>A , CM000666.2:g.52038345T>A GRCh38
NC_000004.11:g.52904511T>A , CM000666.1:g.52904511T>A GRCh37
NC_000004.10:g.52599268T>A NCBI36
NG_008891.1:g.4975A>T , LRG_204:g.4975A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-86A>T ENSP00000370839.5:n.-86A>T