Canonical Allele Identifier: CA2578086720
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038146dup , CM000666.2:g.52038146dup GRCh38
NC_000004.11:g.52904312dup , CM000666.1:g.52904312dup GRCh37
NC_000004.10:g.52599069dup NCBI36
NG_008891.1:g.5175dup , LRG_204:g.5175dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.33+82dup MANE Select ENSP00000370839.6:n.33+82dup
ENST00000381431.9:c.33+82dup ENSP00000370839.5:n.33+82dup
ENST00000506357.5:c.19+82dup
NM_000232.4:c.33+82dup , LRG_204t1:c.33+82dup NP_000223.1:n.33+82dup
XM_011534403.1:c.33+82dup XP_011532705.1:n.33+82dup
NM_000232.5:c.33+82dup MANE Select NP_000223.1:n.33+82dup