Canonical Allele Identifier: CA2147070106
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493510A= , CM000676.2:g.74493510A= GRCh38
NC_000014.8:g.74960213A= , CM000676.1:g.74960213A= GRCh37
NC_000014.7:g.74029966A= NCBI36
NG_007117.1:g.4872T=
NG_033074.1:g.4791A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+60T= ENSP00000450887.1:n.-64+60T=
ENST00000555619.5:c.-236T= ENSP00000451112.1:n.-236T=
ENST00000556009.5:c.147+521T=
NM_001363688.1:c.-236T= NP_001350617.1:n.-236T=
NM_006432.4:c.-236T= NP_006423.1:n.-236T=