Canonical Allele Identifier: CA2670614836
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038369-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038369G>A , CM000666.2:g.52038369G>A GRCh38
NC_000004.11:g.52904535G>A , CM000666.1:g.52904535G>A GRCh37
NC_000004.10:g.52599292G>A NCBI36
NG_008891.1:g.4951C>T , LRG_204:g.4951C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-110C>T ENSP00000370839.5:n.-110C>T