Canonical Allele Identifier: CA2625667508
Gene: NPC2 HGNC NCBI

Linked Data

dbSNP Id: rs2139677049

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493544C>T , CM000676.2:g.74493544C>T GRCh38
NC_000014.8:g.74960247C>T , CM000676.1:g.74960247C>T GRCh37
NC_000014.7:g.74030000C>T NCBI36
NG_007117.1:g.4838G>A
NG_033074.1:g.4825C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+26G>A ENSP00000450887.1:n.-64+26G>A
ENST00000556009.5:c.147+487G>A