Canonical Allele Identifier: CA2670614679
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52038285-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038285T>C , CM000666.2:g.52038285T>C GRCh38
NC_000004.11:g.52904451T>C , CM000666.1:g.52904451T>C GRCh37
NC_000004.10:g.52599208T>C NCBI36
NG_008891.1:g.5035A>G , LRG_204:g.5035A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-26A>G MANE Select ENSP00000370839.6:n.-26A>G
ENST00000381431.9:c.-26A>G ENSP00000370839.5:n.-26A>G
NM_000232.4:c.-26A>G , LRG_204t1:c.-26A>G NP_000223.1:n.-26A>G
XM_011534403.1:c.-26A>G XP_011532705.1:n.-26A>G
NM_000232.5:c.-26A>G MANE Select NP_000223.1:n.-26A>G
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