Canonical Allele Identifier: CA495778414

Gene: NOD2

Linked Data

• MyVariant Identifiers: chr16:g.50733673C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50699762C>G , CM000678.2:g.50699762C>G	GRCh38
NC_000016.9:g.50733673C>G , CM000678.1:g.50733673C>G	GRCh37
NC_000016.8:g.49291174C>G	NCBI36
NG_007508.1:g.7624C>G , LRG_177:g.7624C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.267C>G	ENSP00000493088.1:p.Ser89=
ENST00000646677.2:c.267C>G	ENSP00000496533.1:p.Ser89=
ENST00000641284.1:c.267C>G	ENSP00000493088.1:p.Ser89=
ENST00000646677.1:c.267C>G	ENSP00000496533.1:p.Ser89=
ENST00000647318.2:c.267C>G MANE Select	ENSP00000495993.1:p.Ser89=
ENST00000300589.6:c.348C>G	ENSP00000300589.2:p.Ser116=
ENST00000526417.6:n.335C>G
ENST00000527070.5:c.*963C>G	ENSP00000435149.1:n.*963C>G
ENST00000531674.1:c.267C>G	ENSP00000431681.1:p.Ser89=
ENST00000532206.1:n.452C>G
NM_001293557.1:c.267C>G	NP_001280486.1:p.Ser89=
NM_022162.2:c.348C>G	NP_071445.1:p.Ser116=
XM_005256084.2:c.267C>G	XP_005256141.1:p.Ser89=
XM_006721242.2:c.267C>G	XP_006721305.1:p.Ser89=
XM_006721243.2:c.267C>G	XP_006721306.1:p.Ser89=
XM_011523258.1:c.-38+6100C>G	XP_011521560.1:n.-38+6100C>G
XM_011523259.1:c.-213C>G	XP_011521561.1:n.-213C>G
XM_011523260.1:c.267C>G	XP_011521562.1:p.Ser89=
XM_011523261.1:c.267C>G	XP_011521563.1:p.Ser89=
XR_429725.2:n.357C>G
XR_429726.2:n.357C>G
XR_933387.1:n.357C>G
XM_005256084.4:c.267C>G	XP_005256141.1:p.Ser89=
XM_006721242.4:c.267C>G	XP_006721305.1:p.Ser89=
XM_006721243.4:c.267C>G	XP_006721306.1:p.Ser89=
XM_011523259.2:c.-213C>G	XP_011521561.1:n.-213C>G
XM_011523260.3:c.267C>G	XP_011521562.1:p.Ser89=
XM_011523261.2:c.267C>G	XP_011521563.1:p.Ser89=
XM_017023536.1:c.-127+6100C>G	XP_016879025.1:n.-127+6100C>G
XM_017023537.1:c.-21+6100C>G	XP_016879026.1:n.-21+6100C>G
XR_429725.3:n.310C>G
XR_429726.3:n.310C>G
XR_933387.2:n.310C>G
NM_001293557.2:c.267C>G	NP_001280486.1:p.Ser89=
NM_001370466.1:c.267C>G MANE Select	NP_001357395.1:p.Ser89=
NM_022162.3:c.348C>G	NP_071445.1:p.Ser116=
NR_163434.1:n.332C>G