Canonical Allele Identifier: CA2147070151
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493568A= , CM000676.2:g.74493568A= GRCh38
NC_000014.8:g.74960271A= , CM000676.1:g.74960271A= GRCh37
NC_000014.7:g.74030024A= NCBI36
NG_007117.1:g.4814T=
NG_033074.1:g.4849A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+2T= ENSP00000450887.1:n.-64+2T=
ENST00000556009.5:c.147+463T=