Canonical Allele Identifier: CA15888973
Gene: NOD2 HGNC NCBI

Linked Data

dbSNP Id: rs2076756

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50722970A>G , CM000678.2:g.50722970A>G GRCh38
NC_000016.9:g.50756881A>G , CM000678.1:g.50756881A>G GRCh37
NC_000016.8:g.49314382A>G NCBI36
NG_007508.1:g.30832A>G , LRG_177:g.30832A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000300589.6:c.2798+265A>G ENSP00000300589.2:p.=
NM_001293557.1:c.2717+265A>G NP_001280486.1:p.=
NM_022162.2:c.2798+265A>G NP_071445.1:p.=
XM_005256084.2:c.2717+265A>G XP_005256141.1:p.=
XM_006721242.2:c.2633+265A>G XP_006721305.1:p.=
XM_011523257.1:c.2294+265A>G XP_011521559.1:p.=
XM_011523258.1:c.2294+265A>G XP_011521560.1:p.=
XM_011523259.1:c.2132+265A>G XP_011521561.1:p.=
XM_005256084.4:c.2717+265A>G XP_005256141.1:p.=
XM_006721242.4:c.2633+265A>G XP_006721305.1:p.=
XM_011523259.2:c.2132+265A>G XP_011521561.1:p.=
XM_017023535.1:c.2225+265A>G XP_016879024.1:p.=
XM_017023536.1:c.2132+265A>G XP_016879025.1:p.=
XM_017023537.1:c.2132+265A>G XP_016879026.1:p.=
XM_017023538.1:c.2132+265A>G XP_016879027.1:p.=
NM_001293557.2:c.2717+265A>G NP_001280486.1:p.=
NM_001370466.1:c.2717+265A>G MANE Select NP_001357395.1:p.=
NM_022162.3:c.2798+265A>G NP_071445.1:p.=