Canonical Allele Identifier: CA356875788

Gene: SGCB

Linked Data

• MyVariant Identifiers: chr4:g.52894159A>C (hg19) ; chr4:g.52027993A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52027993A>C , CM000666.2:g.52027993A>C	GRCh38
NC_000004.11:g.52894159A>C , CM000666.1:g.52894159A>C	GRCh37
NC_000004.10:g.52588916A>C	NCBI36
NG_008891.1:g.15327T>G , LRG_204:g.15327T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381431.10:c.728T>G MANE Select	ENSP00000370839.6:p.Met243Arg
ENST00000381431.9:c.728T>G	ENSP00000370839.5:p.Met243Arg
NM_000232.4:c.728T>G , LRG_204t1:c.728T>G	NP_000223.1:p.Met243Arg
XM_006714049.2:c.431T>G	XP_006714112.1:p.Met144Arg
XM_011534403.1:c.518T>G	XP_011532705.1:p.Met173Arg
XM_011534404.1:c.431T>G	XP_011532706.1:p.Met144Arg
NM_000232.5:c.728T>G MANE Select	NP_000223.1:p.Met243Arg