Canonical Allele Identifier: CA3787800
Gene: GLO1 HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.38703061G>A , CM000668.2:g.38703061G>A GRCh38
NC_000006.11:g.38670837G>A , CM000668.1:g.38670837G>A GRCh37
NC_000006.10:g.38778815G>A NCBI36
NG_012074.1:g.5116C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373365.5:c.-7C>T MANE Select ENSP00000362463.3:n.-7C>T
ENST00000373365.4:c.-7C>T ENSP00000362463.3:n.-7C>T
NM_006708.2:c.-7C>T NP_006699.2:n.-7C>T
NM_006708.3:c.-7C>T MANE Select NP_006699.2:n.-7C>T