Canonical Allele Identifier: CA137549359
Gene: GLO1 HGNC NCBI

Linked Data

dbSNP Id: rs746742367
gnomAD v2: 6-38664783-CT-C
gnomAD v3: 6-38697007-CT-C
gnomAD v4: 6-38697007-CT-C
MyVariant Identifiers: chr6:g.38664784del (hg19) chr6:g.38697008del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38697008del , CM000668.2:g.38697008del GRCh38
NC_000006.11:g.38664784del , CM000668.1:g.38664784del GRCh37
NC_000006.10:g.38772762del NCBI36
NG_012074.1:g.11169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.84+5963del MANE Select ENSP00000362463.3:n.84+5963del
ENST00000373365.4:c.84+5963del ENSP00000362463.3:n.84+5963del
NM_006708.2:c.84+5963del NP_006699.2:n.84+5963del
NM_006708.3:c.84+5963del MANE Select NP_006699.2:n.84+5963del
Search 100 bp 5'
Search 100 bp 3'