Canonical Allele Identifier: CA1457434199
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1737457413
gnomAD v4: 4-52038262-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038262T>C , CM000666.2:g.52038262T>C GRCh38
NC_000004.11:g.52904428T>C , CM000666.1:g.52904428T>C GRCh37
NC_000004.10:g.52599185T>C NCBI36
NG_008891.1:g.5058A>G , LRG_204:g.5058A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-3A>G MANE Select ENSP00000370839.6:n.-3A>G
ENST00000381431.9:c.-3A>G ENSP00000370839.5:n.-3A>G
NM_000232.4:c.-3A>G , LRG_204t1:c.-3A>G NP_000223.1:n.-3A>G
XM_011534403.1:c.-3A>G XP_011532705.1:n.-3A>G
NM_000232.5:c.-3A>G MANE Select NP_000223.1:n.-3A>G
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