Canonical Allele Identifier: CA2147070092
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493485C= , CM000676.2:g.74493485C= GRCh38
NC_000014.8:g.74960188C= , CM000676.1:g.74960188C= GRCh37
NC_000014.7:g.74029941C= NCBI36
NG_007117.1:g.4897G=
NG_033074.1:g.4766C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+85G= ENSP00000450887.1:n.-64+85G=
ENST00000555619.5:c.-211G= ENSP00000451112.1:n.-211G=
ENST00000556009.5:c.147+546G=
NM_001363688.1:c.-211G= NP_001350617.1:n.-211G=
NM_006432.4:c.-211G= NP_006423.1:n.-211G=