Canonical Allele Identifier: CA824507547
Gene: GLO1 HGNC NCBI

Linked Data

dbSNP Id: rs1258170396
MyVariant Identifiers: chr6:g.38650535A>T (hg19) chr6:g.38682759A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38682759A>T , CM000668.2:g.38682759A>T GRCh38
NC_000006.11:g.38650535A>T , CM000668.1:g.38650535A>T GRCh37
NC_000006.10:g.38758513A>T NCBI36
NG_012074.1:g.25418T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.376+49T>A MANE Select ENSP00000362463.3:n.376+49T>A
ENST00000373365.4:c.376+49T>A ENSP00000362463.3:n.376+49T>A
ENST00000470973.1:n.408+49T>A
NM_006708.2:c.376+49T>A NP_006699.2:n.376+49T>A
NM_006708.3:c.376+49T>A MANE Select NP_006699.2:n.376+49T>A
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