Canonical Allele Identifier: CA566669765
Gene: GLO1 HGNC NCBI

Linked Data

dbSNP Id: rs1224502896
gnomAD v2: 6-38650803-A-G
gnomAD v3: 6-38683027-A-G
gnomAD v4: 6-38683027-A-G
MyVariant Identifiers: chr6:g.38650803A>G (hg19) chr6:g.38683027A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38683027A>G , CM000668.2:g.38683027A>G GRCh38
NC_000006.11:g.38650803A>G , CM000668.1:g.38650803A>G GRCh37
NC_000006.10:g.38758781A>G NCBI36
NG_012074.1:g.25150T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.309-152T>C MANE Select ENSP00000362463.3:n.309-152T>C
ENST00000373365.4:c.309-152T>C ENSP00000362463.3:n.309-152T>C
ENST00000470973.1:n.189T>C
NM_006708.2:c.309-152T>C NP_006699.2:n.309-152T>C
NM_006708.3:c.309-152T>C MANE Select NP_006699.2:n.309-152T>C
Search 100 bp 5'
Search 100 bp 3'