Canonical Allele Identifier: CA796086457
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1249441231
MyVariant Identifiers: chr4:g.52904463del (hg19) chr4:g.52038297del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038297del , CM000666.2:g.52038297del GRCh38
NC_000004.11:g.52904463del , CM000666.1:g.52904463del GRCh37
NC_000004.10:g.52599220del NCBI36
NG_008891.1:g.5023del , LRG_204:g.5023del

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-38del MANE Select ENSP00000370839.6:n.-38del
ENST00000381431.9:c.-38del ENSP00000370839.5:n.-38del
NM_000232.4:c.-38del , LRG_204t1:c.-38del NP_000223.1:n.-38del
XM_011534403.1:c.-38del XP_011532705.1:n.-38del
NM_000232.5:c.-38del MANE Select NP_000223.1:n.-38del
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