Canonical Allele Identifier: CA1457434212
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737457967
gnomAD v4: 4-52038274-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038274C>G , CM000666.2:g.52038274C>G GRCh38
NC_000004.11:g.52904440C>G , CM000666.1:g.52904440C>G GRCh37
NC_000004.10:g.52599197C>G NCBI36
NG_008891.1:g.5046G>C , LRG_204:g.5046G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-15G>C MANE Select ENSP00000370839.6:n.-15G>C
ENST00000381431.9:c.-15G>C ENSP00000370839.5:n.-15G>C
NM_000232.4:c.-15G>C , LRG_204t1:c.-15G>C NP_000223.1:n.-15G>C
XM_011534403.1:c.-15G>C XP_011532705.1:n.-15G>C
NM_000232.5:c.-15G>C MANE Select NP_000223.1:n.-15G>C
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