Canonical Allele Identifier: CA2147070042
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493392A= , CM000676.2:g.74493392A= GRCh38
NC_000014.8:g.74960095A= , CM000676.1:g.74960095A= GRCh37
NC_000014.7:g.74029848A= NCBI36
NG_007117.1:g.4990T=
NG_033074.1:g.4673A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-63-55T= ENSP00000450887.1:n.-63-55T=
ENST00000555619.5:c.-118T= ENSP00000451112.1:n.-118T=
ENST00000556009.5:c.147+639T=
NM_001363688.1:c.-118T= NP_001350617.1:n.-118T=
NM_006432.4:c.-118T= NP_006423.1:n.-118T=