Canonical Allele Identifier: CA090913
Gene: G6PD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 37123
dbSNP Id: rs1050828

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154536002C>T , CM000685.2:g.154536002C>T GRCh38
NC_000023.10:g.153764217C>T , CM000685.1:g.153764217C>T GRCh37
NC_000023.9:g.153417411C>T NCBI36
NG_009015.2:g.16571G>A

Transcript Alleles

HGVS Amino-acid change
NM_000402.4:c.292G>A VV NP_000393.4:p.Val98Met
NM_001042351.2:c.202G>A VV NP_001035810.1:p.Val68Met
XM_005274657.2:c.292G>A XP_005274714.1:p.Val98Met
XM_005274658.2:c.202G>A XP_005274715.1:p.Val68Met
XM_011531132.1:c.292G>A XP_011529434.1:p.Val98Met
NM_001360016.2:c.202G>A VV NP_001346945.1:p.Val68Met
ENST00000369620.6:c.202G>A ENSP00000358633.2:p.Val68Met
ENST00000393562.6:c.292G>A ENSP00000377192.2:p.Val98Met
ENST00000393564.6:c.202G>A ENSP00000377194.2:p.Val68Met
ENST00000433845.1:c.202G>A ENSP00000394690.1:p.Val68Met
ENST00000439227.5:c.202G>A ENSP00000395599.1:p.Val68Met
ENST00000440967.5:c.202G>A ENSP00000400648.1:p.Val68Met
ENST00000488434.1:n.156G>A
ENST00000497281.5:n.156G>A
ENST00000621232.4:c.202G>A ENSP00000483686.1:p.Val68Met