Canonical Allele Identifier: CA2625667598
Gene: NPC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493585G>C , CM000676.2:g.74493585G>C GRCh38
NC_000014.8:g.74960288G>C , CM000676.1:g.74960288G>C GRCh37
NC_000014.7:g.74030041G>C NCBI36
NG_007117.1:g.4797C>G
NG_033074.1:g.4866G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-79C>G ENSP00000450887.1:n.-79C>G
ENST00000556009.5:c.147+446C>G