Canonical Allele Identifier: CA2466723638
Gene: G6PD HGNC NCBI

Linked Data

dbSNP Id: rs2070362256

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154533162T>C , CM000685.2:g.154533162T>C GRCh38
NC_000023.10:g.153761377T>C , CM000685.1:g.153761377T>C GRCh37
NC_000023.9:g.153414571T>C NCBI36
NG_009015.2:g.19411A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393564.7:c.865-34A>G ENSP00000377194.2:n.865-34A>G
ENST00000439227.6:c.868-34A>G ENSP00000395599.2:n.868-34A>G
ENST00000696420.1:c.865-34A>G ENSP00000512615.1:n.865-34A>G
ENST00000696421.1:c.865-34A>G ENSP00000512616.1:n.865-34A>G
ENST00000696422.1:c.728-34A>G
ENST00000696423.1:c.731-34A>G
ENST00000696424.1:c.717-34A>G ENSP00000512619.1:n.717-34A>G
ENST00000696425.1:c.865-360A>G ENSP00000512620.1:n.865-360A>G
ENST00000696426.1:c.*291A>G ENSP00000512621.1:n.*291A>G
ENST00000696427.1:c.872-34A>G ENSP00000512622.1:n.872-34A>G
ENST00000696428.1:c.*707-34A>G ENSP00000512623.1:n.*707-34A>G
ENST00000696429.1:c.865-34A>G ENSP00000512624.1:n.865-34A>G
ENST00000696430.1:c.865-34A>G ENSP00000512625.1:n.865-34A>G
ENST00000393562.10:c.865-34A>G MANE Select ENSP00000377192.3:n.865-34A>G
ENST00000369620.6:c.1003-34A>G ENSP00000358633.2:n.1003-34A>G
ENST00000393562.6:c.955-34A>G ENSP00000377192.2:n.955-34A>G
ENST00000393564.6:c.865-34A>G ENSP00000377194.2:n.865-34A>G
ENST00000439227.5:c.868-34A>G ENSP00000395599.1:n.868-34A>G
ENST00000440967.5:c.868-34A>G ENSP00000400648.1:n.868-34A>G
ENST00000621232.4:c.865-34A>G ENSP00000483686.1:n.865-34A>G
NM_000402.4:c.955-34A>G NP_000393.4:n.955-34A>G
NM_001042351.2:c.865-34A>G NP_001035810.1:n.865-34A>G
XM_005274657.2:c.958-34A>G XP_005274714.1:n.958-34A>G
XM_005274658.2:c.868-34A>G XP_005274715.1:n.868-34A>G
XM_011531132.1:c.958-360A>G XP_011529434.1:n.958-360A>G
NM_001360016.2:c.865-34A>G MANE Select NP_001346945.1:n.865-34A>G
NM_001042351.3:c.865-34A>G NP_001035810.1:n.865-34A>G