Canonical Allele Identifier: CA1457434022
Gene: SGCB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038045T= , CM000666.2:g.52038045T= GRCh38
NC_000004.11:g.52904211T= , CM000666.1:g.52904211T= GRCh37
NC_000004.10:g.52598968T= NCBI36
NG_008891.1:g.5275A= , LRG_204:g.5275A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+182A= MANE Select ENSP00000370839.6:n.33+182A=
ENST00000381431.9:c.33+182A= ENSP00000370839.5:n.33+182A=
ENST00000506357.5:c.19+182A=
NM_000232.4:c.33+182A= , LRG_204t1:c.33+182A= NP_000223.1:n.33+182A=
XM_011534403.1:c.33+182A= XP_011532705.1:n.33+182A=
NM_000232.5:c.33+182A= MANE Select NP_000223.1:n.33+182A=
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