Canonical Allele Identifier: CA2670614962
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038470-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038470G>T , CM000666.2:g.52038470G>T GRCh38
NC_000004.11:g.52904636G>T , CM000666.1:g.52904636G>T GRCh37
NC_000004.10:g.52599393G>T NCBI36
NG_008891.1:g.4850C>A , LRG_204:g.4850C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-211C>A ENSP00000370839.5:n.-211C>A
Search 100 bp 5'
Search 100 bp 3'