Canonical Allele Identifier: CA356877130

Gene: SGCB

Linked Data

• dbSNP Id: rs1737198271
• MyVariant Identifiers: chr4:g.52895849G>A (hg19) ; chr4:g.52029683G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029683G>A , CM000666.2:g.52029683G>A	GRCh38
NC_000004.11:g.52895849G>A , CM000666.1:g.52895849G>A	GRCh37
NC_000004.10:g.52590606G>A	NCBI36
NG_008891.1:g.13637C>T , LRG_204:g.13637C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000381431.10:c.424C>T MANE Select	ENSP00000370839.6:p.Gln142Ter
ENST00000381431.9:c.424C>T	ENSP00000370839.5:p.Gln142Ter
ENST00000506357.5:c.507C>T
ENST00000514133.1:c.501C>T	ENSP00000425818.1:n.501C>T
NM_000232.4:c.424C>T , LRG_204t1:c.424C>T	NP_000223.1:p.Gln142Ter
XM_006714049.2:c.127C>T	XP_006714112.1:p.Gln43Ter
XM_011534403.1:c.214C>T	XP_011532705.1:p.Gln72Ter
XM_011534404.1:c.127C>T	XP_011532706.1:p.Gln43Ter
NM_000232.5:c.424C>T MANE Select	NP_000223.1:p.Gln142Ter