Canonical Allele Identifier: CA964719459
Gene: NPC2 HGNC NCBI

Linked Data

dbSNP Id: rs1289290410

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493540T>A , CM000676.2:g.74493540T>A GRCh38
NC_000014.8:g.74960243T>A , CM000676.1:g.74960243T>A GRCh37
NC_000014.7:g.74029996T>A NCBI36
NG_007117.1:g.4842A>T
NG_033074.1:g.4821T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+30A>T ENSP00000450887.1:n.-64+30A>T
ENST00000556009.5:c.147+491A>T