Canonical Allele Identifier: CA2147070089
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493483A= , CM000676.2:g.74493483A= GRCh38
NC_000014.8:g.74960186A= , CM000676.1:g.74960186A= GRCh37
NC_000014.7:g.74029939A= NCBI36
NG_007117.1:g.4899T=
NG_033074.1:g.4764A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+87T= ENSP00000450887.1:n.-64+87T=
ENST00000555619.5:c.-209T= ENSP00000451112.1:n.-209T=
ENST00000556009.5:c.147+548T=
NM_001363688.1:c.-209T= NP_001350617.1:n.-209T=
NM_006432.4:c.-209T= NP_006423.1:n.-209T=