Canonical Allele Identifier: CA2625667294

Gene: NPC2

Linked Data

• gnomAD v4: 14-74493444-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.74493444C>A , CM000676.2:g.74493444C>A	GRCh38
NC_000014.8:g.74960147C>A , CM000676.1:g.74960147C>A	GRCh37
NC_000014.7:g.74029900C>A	NCBI36
NG_007117.1:g.4938G>T
NG_033074.1:g.4725C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555592.1:c.-63-107G>T	ENSP00000450887.1:n.-63-107G>T
ENST00000555619.5:c.-170G>T	ENSP00000451112.1:n.-170G>T
ENST00000556009.5:c.147+587G>T
NM_001363688.1:c.-170G>T	NP_001350617.1:n.-170G>T
NM_006432.4:c.-170G>T	NP_006423.1:n.-170G>T