Canonical Allele Identifier: CA964719374
Gene: NPC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493500A>C , CM000676.2:g.74493500A>C GRCh38
NC_000014.8:g.74960203A>C , CM000676.1:g.74960203A>C GRCh37
NC_000014.7:g.74029956A>C NCBI36
NG_007117.1:g.4882T>G
NG_033074.1:g.4781A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+70T>G ENSP00000450887.1:n.-64+70T>G
ENST00000555619.5:c.-226T>G ENSP00000451112.1:n.-226T>G
ENST00000556009.5:c.147+531T>G
NM_001363688.1:c.-226T>G NP_001350617.1:n.-226T>G
NM_006432.4:c.-226T>G NP_006423.1:n.-226T>G