Canonical Allele Identifier: CA450099227
Gene: GLO1 HGNC NCBI

Linked Data

gnomAD v4: 6-38682818-A-G
MyVariant Identifiers: chr6:g.38650594A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000373365.5:c.366T>C MANE Select ENSP00000362463.3:p.Pro122=
ENST00000373365.4:c.366T>C ENSP00000362463.3:p.Pro122=
ENST00000470973.1:n.398T>C
NM_006708.2:c.366T>C NP_006699.2:p.Pro122=
NM_006708.3:c.366T>C MANE Select NP_006699.2:p.Pro122=