Canonical Allele Identifier: CA255481

Linked Data

ClinVar Variation Id: 10694
ClinVar RCV Id: RCV000011440
dbSNP Id: rs104894876

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949873A>C , CM000685.2:g.43949873A>C GRCh38
NC_000023.10:g.43809119A>C , CM000685.1:g.43809119A>C GRCh37
NC_000023.9:g.43694063A>C NCBI36
NG_009832.1:g.28803T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.328T>G (NDP) MANE Select ENSP00000495972.1:p.Cys110Gly
ENST00000647044.1:c.328T>G (NDP) ENSP00000495811.1:p.Cys110Gly
ENST00000378062.5:c.328T>G (NDP) ENSP00000367301.5:p.Cys110Gly
ENST00000470584.1:n.372T>G (NDP)
NM_000266.3:c.328T>G (NDP) NP_000257.1:p.Cys110Gly
NR_046631.1:n.142A>C (NDP-AS1)
NM_000266.4:c.328T>G (NDP) MANE Select NP_000257.1:p.Cys110Gly