Canonical Allele Identifier: CA2670614830
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038364-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038364C>A , CM000666.2:g.52038364C>A GRCh38
NC_000004.11:g.52904530C>A , CM000666.1:g.52904530C>A GRCh37
NC_000004.10:g.52599287C>A NCBI36
NG_008891.1:g.4956G>T , LRG_204:g.4956G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-105G>T ENSP00000370839.5:n.-105G>T