Canonical Allele Identifier: CA551340255
Gene: SGCB HGNC NCBI

Linked Data

dbSNP Id: rs1553940052

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52027866dup , CM000666.2:g.52027866dup GRCh38
NC_000004.11:g.52894032dup , CM000666.1:g.52894032dup GRCh37
NC_000004.10:g.52588789dup NCBI36
NG_008891.1:g.15459dup , LRG_204:g.15459dup

Transcript Alleles

HGVS Amino-acid change
ENST00000381431.10:c.753+107dup MANE Select ENSP00000370839.6:n.753+107dup
ENST00000381431.9:c.753+107dup ENSP00000370839.5:n.753+107dup
NM_000232.4:c.753+107dup , LRG_204t1:c.753+107dup NP_000223.1:n.753+107dup
XM_006714049.2:c.456+107dup XP_006714112.1:n.456+107dup
XM_011534403.1:c.543+107dup XP_011532705.1:n.543+107dup
XM_011534404.1:c.456+107dup XP_011532706.1:n.456+107dup
NM_000232.5:c.753+107dup MANE Select NP_000223.1:n.753+107dup