Canonical Allele Identifier: CA2670614360
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038098-C-CG
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038100dup , CM000666.2:g.52038100dup GRCh38
NC_000004.11:g.52904266dup , CM000666.1:g.52904266dup GRCh37
NC_000004.10:g.52599023dup NCBI36
NG_008891.1:g.5221dup , LRG_204:g.5221dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+128dup MANE Select ENSP00000370839.6:n.33+128dup
ENST00000381431.9:c.33+128dup ENSP00000370839.5:n.33+128dup
ENST00000506357.5:c.19+128dup
NM_000232.4:c.33+128dup , LRG_204t1:c.33+128dup NP_000223.1:n.33+128dup
XM_011534403.1:c.33+128dup XP_011532705.1:n.33+128dup
NM_000232.5:c.33+128dup MANE Select NP_000223.1:n.33+128dup
Search 100 bp 5'
Search 100 bp 3'