Canonical Allele Identifier: CA2670614777
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038332-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038332T>G , CM000666.2:g.52038332T>G GRCh38
NC_000004.11:g.52904498T>G , CM000666.1:g.52904498T>G GRCh37
NC_000004.10:g.52599255T>G NCBI36
NG_008891.1:g.4988A>C , LRG_204:g.4988A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-73A>C ENSP00000370839.5:n.-73A>C