Canonical Allele Identifier: CA356877216

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52895888C>G (hg19) ; chr4:g.52029722C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029722C>G , CM000666.2:g.52029722C>G	GRCh38
NC_000004.11:g.52895888C>G , CM000666.1:g.52895888C>G	GRCh37
NC_000004.10:g.52590645C>G	NCBI36
NG_008891.1:g.13598G>C , LRG_204:g.13598G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.385G>C MANE Select	ENSP00000370839.6:p.Gly129Arg
ENST00000381431.9:c.385G>C	ENSP00000370839.5:p.Gly129Arg
ENST00000506357.5:c.468G>C
ENST00000514133.1:c.462G>C	ENSP00000425818.1:n.462G>C
NM_000232.4:c.385G>C , LRG_204t1:c.385G>C	NP_000223.1:p.Gly129Arg
XM_006714049.2:c.88G>C	XP_006714112.1:p.Gly30Arg
XM_011534403.1:c.175G>C	XP_011532705.1:p.Gly59Arg
XM_011534404.1:c.88G>C	XP_011532706.1:p.Gly30Arg
NM_000232.5:c.385G>C MANE Select	NP_000223.1:p.Gly129Arg