Canonical Allele Identifier: CA442021661
Gene: GLRB HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.158058016T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157136864T>G , CM000666.2:g.157136864T>G GRCh38
NC_000004.11:g.158058016T>G , CM000666.1:g.158058016T>G GRCh37
NC_000004.10:g.158277466T>G NCBI36
NG_015823.1:g.65740T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264428.9:c.588T>G MANE Select ENSP00000264428.4:p.Arg196=
ENST00000264428.8:c.588T>G ENSP00000264428.4:p.Arg196=
ENST00000506411.5:c.*508T>G ENSP00000422039.1:n.*508T>G
ENST00000509282.1:c.588T>G ENSP00000427186.1:p.Arg196=
ENST00000510970.1:n.395T>G
ENST00000512619.5:c.123-33568T>G ENSP00000425433.1:n.123-33568T>G
ENST00000541722.5:c.588T>G ENSP00000441873.1:p.Arg196=
NM_000824.4:c.588T>G NP_000815.1:p.Arg196=
NM_001166060.1:c.588T>G NP_001159532.1:p.Arg196=
NM_001166061.1:c.588T>G NP_001159533.1:p.Arg196=
XM_011531876.1:c.294T>G XP_011530178.1:p.Arg98=
XM_017008034.1:c.294T>G XP_016863523.1:p.Arg98=
XM_017008035.2:c.588T>G XP_016863524.1:p.Arg196=
XR_001741207.2:n.769T>G
XR_002959723.1:n.769T>G
NM_000824.5:c.588T>G MANE Select NP_000815.1:p.Arg196=
NM_001166060.2:c.588T>G NP_001159532.1:p.Arg196=
NM_001166061.2:c.588T>G NP_001159533.1:p.Arg196=