Canonical Allele Identifier: CA2670598600
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52027891-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027893dup , CM000666.2:g.52027893dup GRCh38
NC_000004.11:g.52894059dup , CM000666.1:g.52894059dup GRCh37
NC_000004.10:g.52588816dup NCBI36
NG_008891.1:g.15428dup , LRG_204:g.15428dup

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+76dup MANE Select ENSP00000370839.6:n.753+76dup
ENST00000381431.9:c.753+76dup ENSP00000370839.5:n.753+76dup
NM_000232.4:c.753+76dup , LRG_204t1:c.753+76dup NP_000223.1:n.753+76dup
XM_006714049.2:c.456+76dup XP_006714112.1:n.456+76dup
XM_011534403.1:c.543+76dup XP_011532705.1:n.543+76dup
XM_011534404.1:c.456+76dup XP_011532706.1:n.456+76dup
NM_000232.5:c.753+76dup MANE Select NP_000223.1:n.753+76dup
Search 100 bp 5'
Search 100 bp 3'