Canonical Allele Identifier: CA1062454961
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737463937
gnomAD v3: 4-52038412-A-C
gnomAD v4: 4-52038412-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038412A>C , CM000666.2:g.52038412A>C GRCh38
NC_000004.11:g.52904578A>C , CM000666.1:g.52904578A>C GRCh37
NC_000004.10:g.52599335A>C NCBI36
NG_008891.1:g.4908T>G , LRG_204:g.4908T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-153T>G ENSP00000370839.5:n.-153T>G
Search 100 bp 5'
Search 100 bp 3'