Canonical Allele Identifier: CA796086586
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1427245934
gnomAD v3: 4-52038347-GC-G
gnomAD v4: 4-52038347-GC-G
MyVariant Identifiers: chr4:g.52904514del (hg19) chr4:g.52038348del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038348del , CM000666.2:g.52038348del GRCh38
NC_000004.11:g.52904514del , CM000666.1:g.52904514del GRCh37
NC_000004.10:g.52599271del NCBI36
NG_008891.1:g.4972del , LRG_204:g.4972del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.9:c.-89del ENSP00000370839.5:n.-89del
Search 100 bp 5'
Search 100 bp 3'