Canonical Allele Identifier: CA281275485

Gene: NOD2

Linked Data

• dbSNP Id: rs913605516
• gnomAD v4: 16-50722510-T-C
• MyVariant Identifiers: chr16:g.50756421T>C (hg19) ; chr16:g.50722510T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.50722510T>C , CM000678.2:g.50722510T>C	GRCh38
NC_000016.9:g.50756421T>C , CM000678.1:g.50756421T>C	GRCh37
NC_000016.8:g.49313922T>C	NCBI36
NG_007508.1:g.30372T>C , LRG_177:g.30372T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000641284.2:c.2382-7308T>C	ENSP00000493088.1:n.2382-7308T>C
ENST00000646677.2:c.*399-112T>C	ENSP00000496533.1:n.*399-112T>C
ENST00000697425.1:c.461-112T>C
ENST00000697426.1:c.349-112T>C
ENST00000697427.1:c.265-112T>C
ENST00000697428.1:n.2112-112T>C
ENST00000641284.1:c.2382-7308T>C	ENSP00000493088.1:n.2382-7308T>C
ENST00000646677.1:c.*399-112T>C	ENSP00000496533.1:n.*399-112T>C
ENST00000647318.2:c.2634-112T>C MANE Select	ENSP00000495993.1:n.2634-112T>C
ENST00000300589.6:c.2715-112T>C	ENSP00000300589.2:n.2715-112T>C
ENST00000524712.5:c.209-112T>C
ENST00000527052.5:c.181-112T>C
ENST00000529633.5:c.293-112T>C
ENST00000534057.1:c.349-112T>C
ENST00000534067.5:c.445-112T>C
NM_001293557.1:c.2634-112T>C	NP_001280486.1:n.2634-112T>C
NM_022162.2:c.2715-112T>C	NP_071445.1:n.2715-112T>C
XM_005256084.2:c.2634-112T>C	XP_005256141.1:n.2634-112T>C
XM_006721242.2:c.2550-112T>C	XP_006721305.1:n.2550-112T>C
XM_011523257.1:c.2211-112T>C	XP_011521559.1:n.2211-112T>C
XM_011523258.1:c.2211-112T>C	XP_011521560.1:n.2211-112T>C
XM_011523259.1:c.2049-112T>C	XP_011521561.1:n.2049-112T>C
XR_429725.2:n.2556-112T>C
XR_429726.2:n.2472-112T>C
XR_933387.1:n.2752-112T>C
XM_005256084.4:c.2634-112T>C	XP_005256141.1:n.2634-112T>C
XM_006721242.4:c.2550-112T>C	XP_006721305.1:n.2550-112T>C
XM_011523259.2:c.2049-112T>C	XP_011521561.1:n.2049-112T>C
XM_017023535.1:c.2142-112T>C	XP_016879024.1:n.2142-112T>C
XM_017023536.1:c.2049-112T>C	XP_016879025.1:n.2049-112T>C
XM_017023537.1:c.2049-112T>C	XP_016879026.1:n.2049-112T>C
XM_017023538.1:c.2049-112T>C	XP_016879027.1:n.2049-112T>C
XR_429725.3:n.2509-112T>C
XR_429726.3:n.2425-112T>C
XR_933387.2:n.2705-112T>C
NM_001293557.2:c.2634-112T>C	NP_001280486.1:n.2634-112T>C
NM_001370466.1:c.2634-112T>C MANE Select	NP_001357395.1:n.2634-112T>C
NM_022162.3:c.2715-112T>C	NP_071445.1:n.2715-112T>C
NR_163434.1:n.2846-112T>C