Canonical Allele Identifier: CA2670614635
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038260-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038260C>T , CM000666.2:g.52038260C>T GRCh38
NC_000004.11:g.52904426C>T , CM000666.1:g.52904426C>T GRCh37
NC_000004.10:g.52599183C>T NCBI36
NG_008891.1:g.5060G>A , LRG_204:g.5060G>A

Transcript Alleles

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