Canonical Allele Identifier: CA2147070169
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493601T= , CM000676.2:g.74493601T= GRCh38
NC_000014.8:g.74960304T= , CM000676.1:g.74960304T= GRCh37
NC_000014.7:g.74030057T= NCBI36
NG_007117.1:g.4781A=
NG_033074.1:g.4882T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-95A= ENSP00000450887.1:n.-95A=
ENST00000556009.5:c.147+430A=