Canonical Allele Identifier: CA119854

Gene: SGCB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.52029835C>G , CM000666.2:g.52029835C>G	GRCh38
NC_000004.11:g.52896001C>G , CM000666.1:g.52896001C>G	GRCh37
NC_000004.10:g.52590758C>G	NCBI36
NG_008891.1:g.13485G>C , LRG_204:g.13485G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000232.5:c.272G>C MANE Select	NP_000223.1:p.Arg91Pro
ENST00000381431.10:c.272G>C MANE Select	ENSP00000370839.6:p.Arg91Pro
NM_000232.4:c.272G>C , LRG_204t1:c.272G>C	NP_000223.1:p.Arg91Pro
ENST00000381431.9:c.272G>C	ENSP00000370839.5:p.Arg91Pro
ENST00000506357.5:c.355G>C
ENST00000514133.1:c.349G>C	ENSP00000425818.1:n.349G>C
XM_006714049.2:c.-26G>C	XP_006714112.1:n.-26G>C
XM_011534403.1:c.62G>C	XP_011532705.1:p.Arg21Pro
XM_011534404.1:c.-26G>C	XP_011532706.1:n.-26G>C