Canonical Allele Identifier: CA450099222
Gene: GLO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.38650591T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38682815T>A , CM000668.2:g.38682815T>A GRCh38
NC_000006.11:g.38650591T>A , CM000668.1:g.38650591T>A GRCh37
NC_000006.10:g.38758569T>A NCBI36
NG_012074.1:g.25362A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373365.5:c.369A>T MANE Select ENSP00000362463.3:p.Arg123=
ENST00000373365.4:c.369A>T ENSP00000362463.3:p.Arg123=
ENST00000470973.1:n.401A>T
NM_006708.2:c.369A>T NP_006699.2:p.Arg123=
NM_006708.3:c.369A>T MANE Select NP_006699.2:p.Arg123=
Search 100 bp 5'
Search 100 bp 3'