Canonical Allele Identifier: CA2625667248

Gene: NPC2

Linked Data

• gnomAD v4: 14-74493361-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74493361A>C , CM000676.2:g.74493361A>C	GRCh38
NC_000014.8:g.74960064A>C , CM000676.1:g.74960064A>C	GRCh37
NC_000014.7:g.74029817A>C	NCBI36
NG_007117.1:g.5021T>G
NG_033074.1:g.4642A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555592.1:c.-63-24T>G	ENSP00000450887.1:n.-63-24T>G
ENST00000555619.5:c.-87T>G	ENSP00000451112.1:n.-87T>G
ENST00000556009.5:c.147+670T>G
NM_006432.3:c.-87T>G	NP_006423.1:n.-87T>G
NM_001363688.1:c.-87T>G	NP_001350617.1:n.-87T>G
NM_006432.4:c.-87T>G	NP_006423.1:n.-87T>G