Canonical Allele Identifier: CA566566430
Gene: GLO1 HGNC NCBI

Linked Data

dbSNP Id: rs71744977
gnomAD v2: 6-38664696-CTTTT-C
gnomAD v3: 6-38696920-CTTTT-C
gnomAD v4: 6-38696920-CTTTT-C
MyVariant Identifiers: chr6:g.38664697_38664700del (hg19) chr6:g.38696921_38696924del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38696933_38696936del , CM000668.2:g.38696933_38696936del GRCh38
NC_000006.11:g.38664709_38664712del , CM000668.1:g.38664709_38664712del GRCh37
NC_000006.10:g.38772687_38772690del NCBI36
NG_012074.1:g.11253_11256del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.84+6047_84+6050del MANE Select ENSP00000362463.3:n.84+6047_84+6050del
ENST00000373365.4:c.84+6047_84+6050del ENSP00000362463.3:n.84+6047_84+6050del
NM_006708.2:c.84+6047_84+6050del NP_006699.2:n.84+6047_84+6050del
NM_006708.3:c.84+6047_84+6050del MANE Select NP_006699.2:n.84+6047_84+6050del
Search 100 bp 5'
Search 100 bp 3'