Canonical Allele Identifier: CA1506148503

Gene: GLRB

Linked Data

• dbSNP Id: rs1736419906

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.157136793T>C , CM000666.2:g.157136793T>C	GRCh38
NC_000004.11:g.158057945T>C , CM000666.1:g.158057945T>C	GRCh37
NC_000004.10:g.158277395T>C	NCBI36
NG_015823.1:g.65669T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264428.9:c.528-11T>C MANE Select	ENSP00000264428.4:n.528-11T>C
ENST00000264428.8:c.528-11T>C	ENSP00000264428.4:n.528-11T>C
ENST00000506411.5:c.*448-11T>C	ENSP00000422039.1:n.*448-11T>C
ENST00000509282.1:c.528-11T>C	ENSP00000427186.1:n.528-11T>C
ENST00000510970.1:n.335-11T>C
ENST00000512619.5:c.123-33639T>C	ENSP00000425433.1:n.123-33639T>C
ENST00000541722.5:c.528-11T>C	ENSP00000441873.1:n.528-11T>C
NM_000824.4:c.528-11T>C	NP_000815.1:n.528-11T>C
NM_001166060.1:c.528-11T>C	NP_001159532.1:n.528-11T>C
NM_001166061.1:c.528-11T>C	NP_001159533.1:n.528-11T>C
XM_011531876.1:c.234-11T>C	XP_011530178.1:n.234-11T>C
XM_017008034.1:c.234-11T>C	XP_016863523.1:n.234-11T>C
XM_017008035.2:c.528-11T>C	XP_016863524.1:n.528-11T>C
XR_001741207.2:n.709-11T>C
XR_002959723.1:n.709-11T>C
NM_000824.5:c.528-11T>C MANE Select	NP_000815.1:n.528-11T>C
NM_001166060.2:c.528-11T>C	NP_001159532.1:n.528-11T>C
NM_001166061.2:c.528-11T>C	NP_001159533.1:n.528-11T>C