Canonical Allele Identifier: CA555974119
Gene: GLRB HGNC NCBI

Linked Data

dbSNP Id: rs1214649265

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.157136910A>G , CM000666.2:g.157136910A>G GRCh38
NC_000004.11:g.158058062A>G , CM000666.1:g.158058062A>G GRCh37
NC_000004.10:g.158277512A>G NCBI36
NG_015823.1:g.65786A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264428.9:c.610+24A>G MANE Select ENSP00000264428.4:n.610+24A>G
ENST00000264428.8:c.610+24A>G ENSP00000264428.4:n.610+24A>G
ENST00000506411.5:c.*530+24A>G ENSP00000422039.1:n.*530+24A>G
ENST00000509282.1:c.610+24A>G ENSP00000427186.1:n.610+24A>G
ENST00000510970.1:n.417+24A>G
ENST00000512619.5:c.123-33522A>G ENSP00000425433.1:n.123-33522A>G
ENST00000541722.5:c.610+24A>G ENSP00000441873.1:n.610+24A>G
NM_000824.4:c.610+24A>G NP_000815.1:n.610+24A>G
NM_001166060.1:c.610+24A>G NP_001159532.1:n.610+24A>G
NM_001166061.1:c.610+24A>G NP_001159533.1:n.610+24A>G
XM_011531876.1:c.316+24A>G XP_011530178.1:n.316+24A>G
XM_017008034.1:c.316+24A>G XP_016863523.1:n.316+24A>G
XM_017008035.2:c.610+24A>G XP_016863524.1:n.610+24A>G
XR_001741207.2:n.791+24A>G
XR_002959723.1:n.791+24A>G
NM_000824.5:c.610+24A>G MANE Select NP_000815.1:n.610+24A>G
NM_001166060.2:c.610+24A>G NP_001159532.1:n.610+24A>G
NM_001166061.2:c.610+24A>G NP_001159533.1:n.610+24A>G