Canonical Allele Identifier: CA2670614750
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038319-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038319C>T , CM000666.2:g.52038319C>T GRCh38
NC_000004.11:g.52904485C>T , CM000666.1:g.52904485C>T GRCh37
NC_000004.10:g.52599242C>T NCBI36
NG_008891.1:g.5001G>A , LRG_204:g.5001G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-60G>A ENSP00000370839.5:n.-60G>A
NM_000232.4:c.-60G>A , LRG_204t1:c.-60G>A NP_000223.1:n.-60G>A