Canonical Allele Identifier: CA708507954
Gene: NPC2 HGNC NCBI

Linked Data

dbSNP Id: rs1191294428

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493566G>A , CM000676.2:g.74493566G>A GRCh38
NC_000014.8:g.74960269G>A , CM000676.1:g.74960269G>A GRCh37
NC_000014.7:g.74030022G>A NCBI36
NG_007117.1:g.4816C>T
NG_033074.1:g.4847G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+4C>T ENSP00000450887.1:n.-64+4C>T
ENST00000556009.5:c.147+465C>T