Canonical Allele Identifier: CA2670614850
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038379-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038379T>C , CM000666.2:g.52038379T>C GRCh38
NC_000004.11:g.52904545T>C , CM000666.1:g.52904545T>C GRCh37
NC_000004.10:g.52599302T>C NCBI36
NG_008891.1:g.4941A>G , LRG_204:g.4941A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-120A>G ENSP00000370839.5:n.-120A>G