Canonical Allele Identifier: CA1506148515
Gene: GLRB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157136822A= , CM000666.2:g.157136822A= GRCh38
NC_000004.11:g.158057974A= , CM000666.1:g.158057974A= GRCh37
NC_000004.10:g.158277424A= NCBI36
NG_015823.1:g.65698A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264428.9:c.546A= MANE Select ENSP00000264428.4:p.Ser182=
ENST00000264428.8:c.546A= ENSP00000264428.4:p.Ser182=
ENST00000506411.5:c.*466A= ENSP00000422039.1:n.*466A=
ENST00000509282.1:c.546A= ENSP00000427186.1:p.Ser182=
ENST00000510970.1:n.353A=
ENST00000512619.5:c.123-33610A= ENSP00000425433.1:n.123-33610A=
ENST00000541722.5:c.546A= ENSP00000441873.1:p.Ser182=
NM_000824.4:c.546A= NP_000815.1:p.Ser182=
NM_001166060.1:c.546A= NP_001159532.1:p.Ser182=
NM_001166061.1:c.546A= NP_001159533.1:p.Ser182=
XM_011531876.1:c.252A= XP_011530178.1:p.Ser84=
XM_017008034.1:c.252A= XP_016863523.1:p.Ser84=
XM_017008035.2:c.546A= XP_016863524.1:p.Ser182=
XR_001741207.2:n.727A=
XR_002959723.1:n.727A=
NM_000824.5:c.546A= MANE Select NP_000815.1:p.Ser182=
NM_001166060.2:c.546A= NP_001159532.1:p.Ser182=
NM_001166061.2:c.546A= NP_001159533.1:p.Ser182=