Canonical Allele Identifier: CA2670598939
Gene: SGCB HGNC NCBI

Linked Data

gnomAD v4: 4-52028694-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52028694C>G , CM000666.2:g.52028694C>G GRCh38
NC_000004.11:g.52894860C>G , CM000666.1:g.52894860C>G GRCh37
NC_000004.10:g.52589617C>G NCBI36
NG_008891.1:g.14626G>C , LRG_204:g.14626G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.621+36G>C MANE Select ENSP00000370839.6:n.621+36G>C
ENST00000381431.9:c.621+36G>C ENSP00000370839.5:n.621+36G>C
NM_000232.4:c.621+36G>C , LRG_204t1:c.621+36G>C NP_000223.1:n.621+36G>C
XM_006714049.2:c.324+36G>C XP_006714112.1:n.324+36G>C
XM_011534403.1:c.411+36G>C XP_011532705.1:n.411+36G>C
XM_011534404.1:c.324+36G>C XP_011532706.1:n.324+36G>C
NM_000232.5:c.621+36G>C MANE Select NP_000223.1:n.621+36G>C
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