Canonical Allele Identifier: CA450099228
Gene: GLO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.38650594A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38682818A>T , CM000668.2:g.38682818A>T GRCh38
NC_000006.11:g.38650594A>T , CM000668.1:g.38650594A>T GRCh37
NC_000006.10:g.38758572A>T NCBI36
NG_012074.1:g.25359T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.366T>A MANE Select ENSP00000362463.3:p.Pro122=
ENST00000373365.4:c.366T>A ENSP00000362463.3:p.Pro122=
ENST00000470973.1:n.398T>A
NM_006708.2:c.366T>A NP_006699.2:p.Pro122=
NM_006708.3:c.366T>A MANE Select NP_006699.2:p.Pro122=
Search 100 bp 5'
Search 100 bp 3'