Canonical Allele Identifier: CA358643048
Gene: GLRB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157136881A>C , CM000666.2:g.157136881A>C GRCh38
NC_000004.11:g.158058033A>C , CM000666.1:g.158058033A>C GRCh37
NC_000004.10:g.158277483A>C NCBI36
NG_015823.1:g.65757A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264428.9:c.605A>C MANE Select ENSP00000264428.4:p.Glu202Ala
ENST00000264428.8:c.605A>C ENSP00000264428.4:p.Glu202Ala
ENST00000506411.5:c.*525A>C ENSP00000422039.1:n.*525A>C
ENST00000509282.1:c.605A>C ENSP00000427186.1:p.Glu202Ala
ENST00000510970.1:n.412A>C
ENST00000512619.5:c.123-33551A>C ENSP00000425433.1:n.123-33551A>C
ENST00000541722.5:c.605A>C ENSP00000441873.1:p.Glu202Ala
NM_000824.4:c.605A>C NP_000815.1:p.Glu202Ala
NM_001166060.1:c.605A>C NP_001159532.1:p.Glu202Ala
NM_001166061.1:c.605A>C NP_001159533.1:p.Glu202Ala
XM_011531876.1:c.311A>C XP_011530178.1:p.Glu104Ala
XM_017008034.1:c.311A>C XP_016863523.1:p.Glu104Ala
XM_017008035.2:c.605A>C XP_016863524.1:p.Glu202Ala
XR_001741207.2:n.786A>C
XR_002959723.1:n.786A>C
NM_000824.5:c.605A>C MANE Select NP_000815.1:p.Glu202Ala
NM_001166060.2:c.605A>C NP_001159532.1:p.Glu202Ala
NM_001166061.2:c.605A>C NP_001159533.1:p.Glu202Ala