Canonical Allele Identifier: CA356877482

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52895997A>C (hg19) ; chr4:g.52029831A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029831A>C , CM000666.2:g.52029831A>C	GRCh38
NC_000004.11:g.52895997A>C , CM000666.1:g.52895997A>C	GRCh37
NC_000004.10:g.52590754A>C	NCBI36
NG_008891.1:g.13489T>G , LRG_204:g.13489T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.276T>G MANE Select	ENSP00000370839.6:p.Ile92Met
ENST00000381431.9:c.276T>G	ENSP00000370839.5:p.Ile92Met
ENST00000506357.5:c.359T>G
ENST00000514133.1:c.353T>G	ENSP00000425818.1:n.353T>G
NM_000232.4:c.276T>G , LRG_204t1:c.276T>G	NP_000223.1:p.Ile92Met
XM_006714049.2:c.-22T>G	XP_006714112.1:n.-22T>G
XM_011534403.1:c.66T>G	XP_011532705.1:p.Ile22Met
XM_011534404.1:c.-22T>G	XP_011532706.1:n.-22T>G
NM_000232.5:c.276T>G MANE Select	NP_000223.1:p.Ile92Met