Canonical Allele Identifier: CA2147070116
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493527C= , CM000676.2:g.74493527C= GRCh38
NC_000014.8:g.74960230C= , CM000676.1:g.74960230C= GRCh37
NC_000014.7:g.74029983C= NCBI36
NG_007117.1:g.4855G=
NG_033074.1:g.4808C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+43G= ENSP00000450887.1:n.-64+43G=
ENST00000556009.5:c.147+504G=