Canonical Allele Identifier: CA875556702
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs1402963770
gnomAD v3: X-43949513-T-C
gnomAD v4: X-43949513-T-C
MyVariant Identifiers: chrX:g.43808759T>C (hg19) chrX:g.43949513T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949513T>C , CM000685.2:g.43949513T>C GRCh38
NC_000023.10:g.43808759T>C , CM000685.1:g.43808759T>C GRCh37
NC_000023.9:g.43693703T>C NCBI36
NG_009832.1:g.29163A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*286A>G MANE Select ENSP00000495972.1:n.*286A>G
ENST00000647044.1:c.*286A>G ENSP00000495811.1:n.*286A>G
ENST00000378062.5:c.*286A>G ENSP00000367301.5:n.*286A>G
NM_000266.3:c.*286A>G NP_000257.1:n.*286A>G
NM_000266.4:c.*286A>G MANE Select NP_000257.1:n.*286A>G
Search 100 bp 5'
Search 100 bp 3'