Canonical Allele Identifier: CA13364108
Gene: ANK3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10994359

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60462349T>C , CM000672.2:g.60462349T>C GRCh38
NC_000010.10:g.62222107T>C , CM000672.1:g.62222107T>C GRCh37
NC_000010.9:g.61892113T>C NCBI36
NG_029917.1:g.276178A>G

Transcript Alleles

HGVS Amino-acid change
NM_001204403.1:c.96+152837A>G VV NP_001191332.1:p.=
NM_001204404.1:c.63+110116A>G VV NP_001191333.1:p.=
XM_011539700.1:c.102+152837A>G XP_011538002.1:p.=
XM_011539701.1:c.96+152837A>G XP_011538003.1:p.=
XM_011539702.1:c.58-182710A>G XP_011538004.1:p.=
XM_011539704.1:c.15+35635A>G XP_011538006.1:p.=
XM_017016114.1:c.63+110116A>G XP_016871603.1:p.=
XM_024447958.1:c.63+110116A>G XP_024303726.1:p.=
ENST00000373827.6:c.96+152837A>G ENSP00000362933.2:p.=
ENST00000503366.5:c.63+110116A>G ENSP00000425236.1:p.=
ENST00000622427.4:c.63+110116A>G ENSP00000483244.1:p.=