Canonical Allele Identifier: CA2147070117
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493528C= , CM000676.2:g.74493528C= GRCh38
NC_000014.8:g.74960231C= , CM000676.1:g.74960231C= GRCh37
NC_000014.7:g.74029984C= NCBI36
NG_007117.1:g.4854G=
NG_033074.1:g.4809C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+42G= ENSP00000450887.1:n.-64+42G=
ENST00000556009.5:c.147+503G=