Canonical Allele Identifier: CA1506148551
Gene: GLRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157136909G= , CM000666.2:g.157136909G= GRCh38
NC_000004.11:g.158058061G= , CM000666.1:g.158058061G= GRCh37
NC_000004.10:g.158277511G= NCBI36
NG_015823.1:g.65785G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264428.9:c.610+23G= MANE Select ENSP00000264428.4:n.610+23G=
ENST00000264428.8:c.610+23G= ENSP00000264428.4:n.610+23G=
ENST00000506411.5:c.*530+23G= ENSP00000422039.1:n.*530+23G=
ENST00000509282.1:c.610+23G= ENSP00000427186.1:n.610+23G=
ENST00000510970.1:n.417+23G=
ENST00000512619.5:c.123-33523G= ENSP00000425433.1:n.123-33523G=
ENST00000541722.5:c.610+23G= ENSP00000441873.1:n.610+23G=
NM_000824.4:c.610+23G= NP_000815.1:n.610+23G=
NM_001166060.1:c.610+23G= NP_001159532.1:n.610+23G=
NM_001166061.1:c.610+23G= NP_001159533.1:n.610+23G=
XM_011531876.1:c.316+23G= XP_011530178.1:n.316+23G=
XM_017008034.1:c.316+23G= XP_016863523.1:n.316+23G=
XM_017008035.2:c.610+23G= XP_016863524.1:n.610+23G=
XR_001741207.2:n.791+23G=
XR_002959723.1:n.791+23G=
NM_000824.5:c.610+23G= MANE Select NP_000815.1:n.610+23G=
NM_001166060.2:c.610+23G= NP_001159532.1:n.610+23G=
NM_001166061.2:c.610+23G= NP_001159533.1:n.610+23G=