Canonical Allele Identifier: CA2426745187
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs1244611405
gnomAD v4: X-43949683-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949683C>T , CM000685.2:g.43949683C>T GRCh38
NC_000023.10:g.43808929C>T , CM000685.1:g.43808929C>T GRCh37
NC_000023.9:g.43693873C>T NCBI36
NG_009832.1:g.28993G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.*116G>A MANE Select ENSP00000495972.1:n.*116G>A
ENST00000647044.1:c.*116G>A ENSP00000495811.1:n.*116G>A
ENST00000378062.5:c.*116G>A ENSP00000367301.5:n.*116G>A
ENST00000470584.1:n.562G>A
NM_000266.3:c.*116G>A NP_000257.1:n.*116G>A
NM_000266.4:c.*116G>A MANE Select NP_000257.1:n.*116G>A
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