Canonical Allele Identifier: CA11698032
Gene: ANK2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12500579

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.112934321C>G , CM000666.2:g.112934321C>G GRCh38
NC_000004.10:g.114074926C>G NCBI36
NC_000004.11:g.113855477C>G , CM000666.1:g.113855477C>G GRCh37
NG_009006.2:g.121239C>G , LRG_327:g.121239C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000503271.5:c.21+29807C>G ENSP00000423799.1:p.=
ENST00000503423.5:c.21+29807C>G ENSP00000421011.1:p.=
ENST00000506722.5:c.21+29807C>G ENSP00000421067.1:p.=
NM_001127493.1:c.21+29807C>G , LRG_327t2:c.21+29807C>G NP_001120965.1:p.=
XM_011531891.1:c.21+29807C>G XP_011530193.1:p.=
NM_001127493.2:c.21+29807C>G VV
NM_001354239.1:c.21+29807C>G VV NP_001341168.1:p.=
NM_001354243.1:c.21+29807C>G VV NP_001341172.1:p.=
NM_001354244.1:c.21+29807C>G VV NP_001341173.1:p.=
NM_001354249.1:c.21+29807C>G VV NP_001341178.1:p.=
NM_001354252.1:c.21+29807C>G VV NP_001341181.1:p.=
NM_001354253.1:c.21+29807C>G VV NP_001341182.1:p.=
NM_001354254.1:c.21+29807C>G VV NP_001341183.1:p.=
NM_001354255.1:c.21+29807C>G VV NP_001341184.1:p.=
NM_001354256.1:c.21+29807C>G VV NP_001341185.1:p.=
NM_001354257.1:c.21+29807C>G VV NP_001341186.1:p.=
NM_001354260.1:c.21+29807C>G VV NP_001341189.1:p.=
NM_001354261.1:c.21+29807C>G VV NP_001341190.1:p.=
NM_001354262.1:c.21+29807C>G VV NP_001341191.1:p.=
NM_001354264.1:c.21+29807C>G VV NP_001341193.1:p.=
NM_001354266.1:c.21+29807C>G VV NP_001341195.1:p.=
NM_001354267.1:c.21+29807C>G VV NP_001341196.1:p.=
NM_001354269.1:c.72+228104C>G VV NP_001341198.1:p.=
NM_001354270.1:c.21+29807C>G VV NP_001341199.1:p.=
NM_001354271.1:c.21+29807C>G VV NP_001341200.1:p.=
NM_001354272.1:c.21+29807C>G VV NP_001341201.1:p.=
NM_001354274.1:c.21+29807C>G VV NP_001341203.1:p.=
NM_001354275.1:c.21+29807C>G VV NP_001341204.1:p.=
NM_001354276.1:c.21+29807C>G VV NP_001341205.1:p.=
NM_001354277.1:c.21+29807C>G VV NP_001341206.1:p.=
XM_017008071.2:c.21+29807C>G XP_016863560.1:p.=
XM_017008072.2:c.21+29807C>G XP_016863561.1:p.=
XM_017008074.2:c.21+29807C>G XP_016863563.1:p.=
XM_017008075.2:c.21+29807C>G XP_016863564.1:p.=
XM_017008077.2:c.21+29807C>G XP_016863566.1:p.=
XM_017008080.2:c.21+29807C>G XP_016863569.1:p.=