Canonical Allele Identifier: CA964719340
Gene: NPC2 HGNC NCBI

Linked Data

dbSNP Id: rs2086801642

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493461G>A , CM000676.2:g.74493461G>A GRCh38
NC_000014.8:g.74960164G>A , CM000676.1:g.74960164G>A GRCh37
NC_000014.7:g.74029917G>A NCBI36
NG_007117.1:g.4921C>T
NG_033074.1:g.4742G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+109C>T ENSP00000450887.1:n.-64+109C>T
ENST00000555619.5:c.-187C>T ENSP00000451112.1:n.-187C>T
ENST00000556009.5:c.147+570C>T
NM_001363688.1:c.-187C>T NP_001350617.1:n.-187C>T
NM_006432.4:c.-187C>T NP_006423.1:n.-187C>T