Canonical Allele Identifier: CA2147070158
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493584G= , CM000676.2:g.74493584G= GRCh38
NC_000014.8:g.74960287G= , CM000676.1:g.74960287G= GRCh37
NC_000014.7:g.74030040G= NCBI36
NG_007117.1:g.4798C=
NG_033074.1:g.4865G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-78C= ENSP00000450887.1:n.-78C=
ENST00000556009.5:c.147+447C=