Canonical Allele Identifier: CA356875779

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52894154C>A (hg19) ; chr4:g.52027988C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52027988C>A , CM000666.2:g.52027988C>A	GRCh38
NC_000004.11:g.52894154C>A , CM000666.1:g.52894154C>A	GRCh37
NC_000004.10:g.52588911C>A	NCBI36
NG_008891.1:g.15332G>T , LRG_204:g.15332G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.733G>T MANE Select	ENSP00000370839.6:p.Gly245Cys
ENST00000381431.9:c.733G>T	ENSP00000370839.5:p.Gly245Cys
NM_000232.4:c.733G>T , LRG_204t1:c.733G>T	NP_000223.1:p.Gly245Cys
XM_006714049.2:c.436G>T	XP_006714112.1:p.Gly146Cys
XM_011534403.1:c.523G>T	XP_011532705.1:p.Gly175Cys
XM_011534404.1:c.436G>T	XP_011532706.1:p.Gly146Cys
NM_000232.5:c.733G>T MANE Select	NP_000223.1:p.Gly245Cys