Canonical Allele Identifier: CA2741390379
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493429G>A , CM000676.2:g.74493429G>A GRCh38
NC_000014.8:g.74960132G>A , CM000676.1:g.74960132G>A GRCh37
NC_000014.7:g.74029885G>A NCBI36
NG_007117.1:g.4953C>T
NG_033074.1:g.4710G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-63-92C>T ENSP00000450887.1:n.-63-92C>T
ENST00000555619.5:c.-155C>T ENSP00000451112.1:n.-155C>T
ENST00000556009.5:c.147+602C>T
NM_001363688.1:c.-155C>T NP_001350617.1:n.-155C>T
NM_006432.4:c.-155C>T NP_006423.1:n.-155C>T