Canonical Allele Identifier: CA2147070152
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493573T= , CM000676.2:g.74493573T= GRCh38
NC_000014.8:g.74960276T= , CM000676.1:g.74960276T= GRCh37
NC_000014.7:g.74030029T= NCBI36
NG_007117.1:g.4809A=
NG_033074.1:g.4854T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-67A= ENSP00000450887.1:n.-67A=
ENST00000556009.5:c.147+458A=