Canonical Allele Identifier: CA10566088

Gene: G6PD

Linked Data

• dbSNP Id: rs781808013
• ExAC: X:153761056 C / A
• gnomAD v2: X-153761056-C-A
• gnomAD v4: X-154532841-C-A
• MyVariant Identifiers: chrX:g.153761056C>A (hg19) ; chrX:g.154532841C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154532841C>A , CM000685.2:g.154532841C>A	GRCh38
NC_000023.10:g.153761056C>A , CM000685.1:g.153761056C>A	GRCh37
NC_000023.9:g.153414250C>A	NCBI36
NG_009015.2:g.19732G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393564.7:c.1052-39G>T	ENSP00000377194.2:n.1052-39G>T
ENST00000439227.6:c.1055-39G>T	ENSP00000395599.2:n.1055-39G>T
ENST00000696420.1:c.1052-39G>T	ENSP00000512615.1:n.1052-39G>T
ENST00000696421.1:c.1052-39G>T	ENSP00000512616.1:n.1052-39G>T
ENST00000696422.1:c.915-39G>T
ENST00000696423.1:c.918-39G>T
ENST00000696424.1:c.904-39G>T	ENSP00000512619.1:n.904-39G>T
ENST00000696425.1:c.865-39G>T	ENSP00000512620.1:n.865-39G>T
ENST00000696426.1:c.*512-39G>T	ENSP00000512621.1:n.*512-39G>T
ENST00000696427.1:c.*12-39G>T	ENSP00000512622.1:n.*12-39G>T
ENST00000696428.1:c.*894-39G>T	ENSP00000512623.1:n.*894-39G>T
ENST00000696429.1:c.1052-39G>T	ENSP00000512624.1:n.1052-39G>T
ENST00000696430.1:c.1052-39G>T	ENSP00000512625.1:n.1052-39G>T
ENST00000393562.10:c.1052-39G>T MANE Select	ENSP00000377192.3:n.1052-39G>T
ENST00000369620.6:c.1190-39G>T	ENSP00000358633.2:n.1190-39G>T
ENST00000393562.6:c.1142-39G>T	ENSP00000377192.2:n.1142-39G>T
ENST00000393564.6:c.1052-39G>T	ENSP00000377194.2:n.1052-39G>T
ENST00000490651.1:n.234G>T
ENST00000621232.4:c.1052-39G>T	ENSP00000483686.1:n.1052-39G>T
NM_000402.4:c.1142-39G>T	NP_000393.4:n.1142-39G>T
NM_001042351.2:c.1052-39G>T	NP_001035810.1:n.1052-39G>T
XM_005274657.2:c.1145-39G>T	XP_005274714.1:n.1145-39G>T
XM_005274658.2:c.1055-39G>T	XP_005274715.1:n.1055-39G>T
XM_011531132.1:c.958-39G>T	XP_011529434.1:n.958-39G>T
NM_001360016.2:c.1052-39G>T MANE Select	NP_001346945.1:n.1052-39G>T
NM_001042351.3:c.1052-39G>T	NP_001035810.1:n.1052-39G>T