Canonical Allele Identifier: CA3787676
Gene: GLO1 HGNC NCBI

Linked Data

dbSNP Id: rs556956668
ExAC: 6:38650558 T / C
gnomAD v2: 6-38650558-T-C
gnomAD v3: 6-38682782-T-C
gnomAD v4: 6-38682782-T-C
MyVariant Identifiers: chr6:g.38650558T>C (hg19) chr6:g.38682782T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38682782T>C , CM000668.2:g.38682782T>C GRCh38
NC_000006.11:g.38650558T>C , CM000668.1:g.38650558T>C GRCh37
NC_000006.10:g.38758536T>C NCBI36
NG_012074.1:g.25395A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.376+26A>G MANE Select ENSP00000362463.3:n.376+26A>G
ENST00000373365.4:c.376+26A>G ENSP00000362463.3:n.376+26A>G
ENST00000470973.1:n.408+26A>G
NM_006708.2:c.376+26A>G NP_006699.2:n.376+26A>G
NM_006708.3:c.376+26A>G MANE Select NP_006699.2:n.376+26A>G
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