Canonical Allele Identifier: CA1506148520

Gene: GLRB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.157136827C= , CM000666.2:g.157136827C=	GRCh38
NC_000004.11:g.158057979C= , CM000666.1:g.158057979C=	GRCh37
NC_000004.10:g.158277429C=	NCBI36
NG_015823.1:g.65703C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264428.9:c.551C= MANE Select	ENSP00000264428.4:p.Pro184=
ENST00000264428.8:c.551C=	ENSP00000264428.4:p.Pro184=
ENST00000506411.5:c.*471C=	ENSP00000422039.1:n.*471C=
ENST00000509282.1:c.551C=	ENSP00000427186.1:p.Pro184=
ENST00000510970.1:n.358C=
ENST00000512619.5:c.123-33605C=	ENSP00000425433.1:n.123-33605C=
ENST00000541722.5:c.551C=	ENSP00000441873.1:p.Pro184=
NM_000824.4:c.551C=	NP_000815.1:p.Pro184=
NM_001166060.1:c.551C=	NP_001159532.1:p.Pro184=
NM_001166061.1:c.551C=	NP_001159533.1:p.Pro184=
XM_011531876.1:c.257C=	XP_011530178.1:p.Pro86=
XM_017008034.1:c.257C=	XP_016863523.1:p.Pro86=
XM_017008035.2:c.551C=	XP_016863524.1:p.Pro184=
XR_001741207.2:n.732C=
XR_002959723.1:n.732C=
NM_000824.5:c.551C= MANE Select	NP_000815.1:p.Pro184=
NM_001166060.2:c.551C=	NP_001159532.1:p.Pro184=
NM_001166061.2:c.551C=	NP_001159533.1:p.Pro184=