Canonical Allele Identifier: CA2670614967
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038476-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038476G>T , CM000666.2:g.52038476G>T GRCh38
NC_000004.11:g.52904642G>T , CM000666.1:g.52904642G>T GRCh37
NC_000004.10:g.52599399G>T NCBI36
NG_008891.1:g.4844C>A , LRG_204:g.4844C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-217C>A ENSP00000370839.5:n.-217C>A