Canonical Allele Identifier: CA2670614771
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038330-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038330C>T , CM000666.2:g.52038330C>T GRCh38
NC_000004.11:g.52904496C>T , CM000666.1:g.52904496C>T GRCh37
NC_000004.10:g.52599253C>T NCBI36
NG_008891.1:g.4990G>A , LRG_204:g.4990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-71G>A ENSP00000370839.5:n.-71G>A
Search 100 bp 5'
Search 100 bp 3'