Canonical Allele Identifier: CA1132659300
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs2035747991
gnomAD v3: X-43949516-T-C
gnomAD v4: X-43949516-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949516T>C , CM000685.2:g.43949516T>C GRCh38
NC_000023.10:g.43808762T>C , CM000685.1:g.43808762T>C GRCh37
NC_000023.9:g.43693706T>C NCBI36
NG_009832.1:g.29160A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*283A>G MANE Select ENSP00000495972.1:n.*283A>G
ENST00000647044.1:c.*283A>G ENSP00000495811.1:n.*283A>G
ENST00000378062.5:c.*283A>G ENSP00000367301.5:n.*283A>G
NM_000266.3:c.*283A>G NP_000257.1:n.*283A>G
NM_000266.4:c.*283A>G MANE Select NP_000257.1:n.*283A>G
Search 100 bp 5'
Search 100 bp 3'