Canonical Allele Identifier: CA1131417968
Gene: PHKA2 HGNC NCBI

Linked Data

dbSNP Id: rs778882246
gnomAD v3: X-18951094-C-G
gnomAD v4: X-18951094-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.18951094C>G , CM000685.2:g.18951094C>G GRCh38
NC_000023.10:g.18969212C>G , CM000685.1:g.18969212C>G GRCh37
NC_000023.9:g.18879133C>G NCBI36
NG_016622.1:g.38269G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000379942.5:c.454+10G>C MANE Select ENSP00000369274.4:n.454+10G>C
ENST00000379942.4:c.454+10G>C ENSP00000369274.4:n.454+10G>C
NM_000292.2:c.454+10G>C NP_000283.1:n.454+10G>C
XM_005274548.3:c.454+10G>C XP_005274605.1:n.454+10G>C
XM_005274550.3:c.454+10G>C XP_005274607.1:n.454+10G>C
XM_006724496.2:c.454+10G>C XP_006724559.1:n.454+10G>C
XM_006724498.2:c.-93+1400G>C XP_006724561.1:n.-93+1400G>C
XM_011545537.1:c.454+10G>C XP_011543839.1:n.454+10G>C
XR_950461.1:n.638+10G>C
XM_005274548.5:c.454+10G>C XP_005274605.1:n.454+10G>C
XM_005274550.5:c.454+10G>C XP_005274607.1:n.454+10G>C
XM_006724496.4:c.454+10G>C XP_006724559.1:n.454+10G>C
XM_006724498.4:c.-93+1400G>C XP_006724561.1:n.-93+1400G>C
XM_011545537.3:c.454+10G>C XP_011543839.1:n.454+10G>C
XM_017029580.2:c.-388+10G>C XP_016885069.1:n.-388+10G>C
XR_001755697.2:n.624+10G>C
XR_001755698.2:n.624+10G>C
XR_002958777.1:n.624+10G>C
XR_950461.3:n.624+10G>C
NM_000292.3:c.454+10G>C MANE Select NP_000283.1:n.454+10G>C