Canonical Allele Identifier: CA96791935
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs10434429
gnomAD v2: 4-52904614-C-T
gnomAD v3: 4-52038448-C-T
gnomAD v4: 4-52038448-C-T
MyVariant Identifiers: chr4:g.52904614C>T (hg19) chr4:g.52038448C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038448C>T , CM000666.2:g.52038448C>T GRCh38
NC_000004.11:g.52904614C>T , CM000666.1:g.52904614C>T GRCh37
NC_000004.10:g.52599371C>T NCBI36
NG_008891.1:g.4872G>A , LRG_204:g.4872G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-189G>A ENSP00000370839.5:n.-189G>A
Search 100 bp 5'
Search 100 bp 3'