Canonical Allele Identifier: CA2147070035

Gene: NPC2

Linked Data

• dbSNP Id: rs2086800316

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74493379G>A , CM000676.2:g.74493379G>A	GRCh38
NC_000014.8:g.74960082G>A , CM000676.1:g.74960082G>A	GRCh37
NC_000014.7:g.74029835G>A	NCBI36
NG_007117.1:g.5003C>T
NG_033074.1:g.4660G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555592.1:c.-63-42C>T	ENSP00000450887.1:n.-63-42C>T
ENST00000555619.5:c.-105C>T	ENSP00000451112.1:n.-105C>T
ENST00000556009.5:c.147+652C>T
NM_006432.3:c.-105C>T	NP_006423.1:n.-105C>T
NM_001363688.1:c.-105C>T	NP_001350617.1:n.-105C>T
NM_006432.4:c.-105C>T	NP_006423.1:n.-105C>T