Canonical Allele Identifier: CA439273639

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52894167T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028001T>C , CM000666.2:g.52028001T>C	GRCh38
NC_000004.11:g.52894167T>C , CM000666.1:g.52894167T>C	GRCh37
NC_000004.10:g.52588924T>C	NCBI36
NG_008891.1:g.15319A>G , LRG_204:g.15319A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.720A>G MANE Select	ENSP00000370839.6:p.Glu240=
ENST00000381431.9:c.720A>G	ENSP00000370839.5:p.Glu240=
NM_000232.4:c.720A>G , LRG_204t1:c.720A>G	NP_000223.1:p.Glu240=
XM_006714049.2:c.423A>G	XP_006714112.1:p.Glu141=
XM_011534403.1:c.510A>G	XP_011532705.1:p.Glu170=
XM_011534404.1:c.423A>G	XP_011532706.1:p.Glu141=
NM_000232.5:c.720A>G MANE Select	NP_000223.1:p.Glu240=