Canonical Allele Identifier: CA439273742

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52894191T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52028025T>A , CM000666.2:g.52028025T>A	GRCh38
NC_000004.11:g.52894191T>A , CM000666.1:g.52894191T>A	GRCh37
NC_000004.10:g.52588948T>A	NCBI36
NG_008891.1:g.15295A>T , LRG_204:g.15295A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.696A>T MANE Select	ENSP00000370839.6:p.Val232=
ENST00000381431.9:c.696A>T	ENSP00000370839.5:p.Val232=
NM_000232.4:c.696A>T , LRG_204t1:c.696A>T	NP_000223.1:p.Val232=
XM_006714049.2:c.399A>T	XP_006714112.1:p.Val133=
XM_011534403.1:c.486A>T	XP_011532705.1:p.Val162=
XM_011534404.1:c.399A>T	XP_011532706.1:p.Val133=
NM_000232.5:c.696A>T MANE Select	NP_000223.1:p.Val232=