Canonical Allele Identifier: CA1457434263
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1301409435
gnomAD v4: 4-52038329-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038329G>A , CM000666.2:g.52038329G>A GRCh38
NC_000004.11:g.52904495G>A , CM000666.1:g.52904495G>A GRCh37
NC_000004.10:g.52599252G>A NCBI36
NG_008891.1:g.4991C>T , LRG_204:g.4991C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-70C>T ENSP00000370839.5:n.-70C>T