Canonical Allele Identifier: CA2670614761
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038324-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038324T>A , CM000666.2:g.52038324T>A GRCh38
NC_000004.11:g.52904490T>A , CM000666.1:g.52904490T>A GRCh37
NC_000004.10:g.52599247T>A NCBI36
NG_008891.1:g.4996A>T , LRG_204:g.4996A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-65A>T ENSP00000370839.5:n.-65A>T
Search 100 bp 5'
Search 100 bp 3'