Canonical Allele Identifier: CA1457434015
Gene: SGCB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038040T= , CM000666.2:g.52038040T= GRCh38
NC_000004.11:g.52904206T= , CM000666.1:g.52904206T= GRCh37
NC_000004.10:g.52598963T= NCBI36
NG_008891.1:g.5280A= , LRG_204:g.5280A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+187A= MANE Select ENSP00000370839.6:n.33+187A=
ENST00000381431.9:c.33+187A= ENSP00000370839.5:n.33+187A=
ENST00000506357.5:c.19+187A=
NM_000232.4:c.33+187A= , LRG_204t1:c.33+187A= NP_000223.1:n.33+187A=
XM_011534403.1:c.33+187A= XP_011532705.1:n.33+187A=
NM_000232.5:c.33+187A= MANE Select NP_000223.1:n.33+187A=
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