Canonical Allele Identifier: CA575416

Gene: H6PD

Linked Data

• dbSNP Id: rs751449332
• ExAC: 1:9324327 G / T
• gnomAD v2: 1-9324327-G-T
• gnomAD v3: 1-9264268-G-T
• gnomAD v4: 1-9264268-G-T
• MyVariant Identifiers: chr1:g.9324327G>T (hg19) ; chr1:g.9264268G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.9264268G>T , CM000663.2:g.9264268G>T	GRCh38
NC_000001.10:g.9324327G>T , CM000663.1:g.9324327G>T	GRCh37
NC_000001.9:g.9246914G>T	NCBI36
NG_012218.1:g.34465G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377403.7:c.1775G>T MANE Select	ENSP00000366620.2:p.Gly592Val
ENST00000377403.6:c.1775G>T	ENSP00000366620.1:p.Gly592Val
ENST00000602477.1:c.1808G>T	ENSP00000473348.1:p.Gly603Val
NM_001282587.1:c.1808G>T	NP_001269516.1:p.Gly603Val
NM_004285.3:c.1775G>T	NP_004276.2:p.Gly592Val
XM_005263539.3:c.1808G>T	XP_005263596.1:p.Gly603Val
XM_005263540.3:c.1802G>T	XP_005263597.1:p.Gly601Val
XM_006711052.2:c.1775G>T	XP_006711115.1:p.Gly592Val
XM_011542446.1:c.1775G>T	XP_011540748.1:p.Gly592Val
XM_005263540.5:c.1802G>T	XP_005263597.1:p.Gly601Val
XM_006711052.4:c.1775G>T	XP_006711115.1:p.Gly592Val
XM_017002865.2:c.1775G>T	XP_016858354.1:p.Gly592Val
XM_017002866.2:c.707G>T	XP_016858355.1:p.Gly236Val
NM_001282587.2:c.1808G>T	NP_001269516.1:p.Gly603Val
NM_004285.4:c.1775G>T MANE Select	NP_004276.2:p.Gly592Val