Canonical Allele Identifier: CA2147070131
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493552T= , CM000676.2:g.74493552T= GRCh38
NC_000014.8:g.74960255T= , CM000676.1:g.74960255T= GRCh37
NC_000014.7:g.74030008T= NCBI36
NG_007117.1:g.4830A=
NG_033074.1:g.4833T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+18A= ENSP00000450887.1:n.-64+18A=
ENST00000556009.5:c.147+479A=