Canonical Allele Identifier: CA2738362028
Gene: NDP HGNC NCBI

Linked Data

dbSNP Id: rs369137059

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949601G>C , CM000685.2:g.43949601G>C GRCh38
NC_000023.10:g.43808847G>C , CM000685.1:g.43808847G>C GRCh37
NC_000023.9:g.43693791G>C NCBI36
NG_009832.1:g.29075C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*198C>G MANE Select ENSP00000495972.1:n.*198C>G
ENST00000647044.1:c.*198C>G ENSP00000495811.1:n.*198C>G
ENST00000378062.5:c.*198C>G ENSP00000367301.5:n.*198C>G
NM_000266.3:c.*198C>G NP_000257.1:n.*198C>G
NM_000266.4:c.*198C>G MANE Select NP_000257.1:n.*198C>G