Canonical Allele Identifier: CA2831038879
Gene: SGCB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038251_52038270dup , CM000666.2:g.52038251_52038270dup GRCh38
NC_000004.11:g.52904417_52904436dup , CM000666.1:g.52904417_52904436dup GRCh37
NC_000004.10:g.52599174_52599193dup NCBI36
NG_008891.1:g.5051_5070dup , LRG_204:g.5051_5070dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-10_10dup MANE Select ENSP00000370839.6:p.Ala4GlyfsTer22
ENST00000381431.9:c.-10_10dup ENSP00000370839.5:p.Ala4GlyfsTer22
NM_000232.4:c.-10_10dup , LRG_204t1:c.-10_10dup NP_000223.1:p.Ala4GlyfsTer22
XM_011534403.1:c.-10_10dup XP_011532705.1:p.Ala4GlyfsTer16
NM_000232.5:c.-10_10dup MANE Select NP_000223.1:p.Ala4GlyfsTer22
Search 100 bp 5'
Search 100 bp 3'