Canonical Allele Identifier: CA356876059

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52894210A>C (hg19) ; chr4:g.52028044A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028044A>C , CM000666.2:g.52028044A>C	GRCh38
NC_000004.11:g.52894210A>C , CM000666.1:g.52894210A>C	GRCh37
NC_000004.10:g.52588967A>C	NCBI36
NG_008891.1:g.15276T>G , LRG_204:g.15276T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.677T>G MANE Select	ENSP00000370839.6:p.Val226Gly
ENST00000381431.9:c.677T>G	ENSP00000370839.5:p.Val226Gly
NM_000232.4:c.677T>G , LRG_204t1:c.677T>G	NP_000223.1:p.Val226Gly
XM_006714049.2:c.380T>G	XP_006714112.1:p.Val127Gly
XM_011534403.1:c.467T>G	XP_011532705.1:p.Val156Gly
XM_011534404.1:c.380T>G	XP_011532706.1:p.Val127Gly
NM_000232.5:c.677T>G MANE Select	NP_000223.1:p.Val226Gly