Canonical Allele Identifier: CA2147070145
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493563A= , CM000676.2:g.74493563A= GRCh38
NC_000014.8:g.74960266A= , CM000676.1:g.74960266A= GRCh37
NC_000014.7:g.74030019A= NCBI36
NG_007117.1:g.4819T=
NG_033074.1:g.4844A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+7T= ENSP00000450887.1:n.-64+7T=
ENST00000556009.5:c.147+468T=