Canonical Allele Identifier: CA1457434052
Gene: SGCB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038075C= , CM000666.2:g.52038075C= GRCh38
NC_000004.11:g.52904241C= , CM000666.1:g.52904241C= GRCh37
NC_000004.10:g.52598998C= NCBI36
NG_008891.1:g.5245G= , LRG_204:g.5245G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+152G= MANE Select ENSP00000370839.6:n.33+152G=
ENST00000381431.9:c.33+152G= ENSP00000370839.5:n.33+152G=
ENST00000506357.5:c.19+152G=
NM_000232.4:c.33+152G= , LRG_204t1:c.33+152G= NP_000223.1:n.33+152G=
XM_011534403.1:c.33+152G= XP_011532705.1:n.33+152G=
NM_000232.5:c.33+152G= MANE Select NP_000223.1:n.33+152G=
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