Canonical Allele Identifier: CA824507839
Gene: GLO1 HGNC NCBI

Linked Data

dbSNP Id: rs1302753196
gnomAD v3: 6-38683063-A-G
gnomAD v4: 6-38683063-A-G
MyVariant Identifiers: chr6:g.38650839A>G (hg19) chr6:g.38683063A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38683063A>G , CM000668.2:g.38683063A>G GRCh38
NC_000006.11:g.38650839A>G , CM000668.1:g.38650839A>G GRCh37
NC_000006.10:g.38758817A>G NCBI36
NG_012074.1:g.25114T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.309-188T>C MANE Select ENSP00000362463.3:n.309-188T>C
ENST00000373365.4:c.309-188T>C ENSP00000362463.3:n.309-188T>C
ENST00000470973.1:n.153T>C
NM_006708.2:c.309-188T>C NP_006699.2:n.309-188T>C
NM_006708.3:c.309-188T>C MANE Select NP_006699.2:n.309-188T>C
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