Canonical Allele Identifier: CA2670614961
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038469-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038469G>T , CM000666.2:g.52038469G>T GRCh38
NC_000004.11:g.52904635G>T , CM000666.1:g.52904635G>T GRCh37
NC_000004.10:g.52599392G>T NCBI36
NG_008891.1:g.4851C>A , LRG_204:g.4851C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-210C>A ENSP00000370839.5:n.-210C>A