Canonical Allele Identifier: CA137714954
Gene: GLO1 HGNC NCBI

Linked Data

dbSNP Id: rs915014512
gnomAD v4: 6-38683040-C-T
MyVariant Identifiers: chr6:g.38650816C>T (hg19) chr6:g.38683040C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38683040C>T , CM000668.2:g.38683040C>T GRCh38
NC_000006.11:g.38650816C>T , CM000668.1:g.38650816C>T GRCh37
NC_000006.10:g.38758794C>T NCBI36
NG_012074.1:g.25137G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.309-165G>A MANE Select ENSP00000362463.3:n.309-165G>A
ENST00000373365.4:c.309-165G>A ENSP00000362463.3:n.309-165G>A
ENST00000470973.1:n.176G>A
NM_006708.2:c.309-165G>A NP_006699.2:n.309-165G>A
NM_006708.3:c.309-165G>A MANE Select NP_006699.2:n.309-165G>A
Search 100 bp 5'
Search 100 bp 3'