Canonical Allele Identifier: CA964719433
Gene: NPC2 HGNC NCBI

Linked Data

dbSNP Id: rs1328708800
gnomAD v3: 14-74493533-T-A
gnomAD v4: 14-74493533-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493533T>A , CM000676.2:g.74493533T>A GRCh38
NC_000014.8:g.74960236T>A , CM000676.1:g.74960236T>A GRCh37
NC_000014.7:g.74029989T>A NCBI36
NG_007117.1:g.4849A>T
NG_033074.1:g.4814T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+37A>T ENSP00000450887.1:n.-64+37A>T
ENST00000556009.5:c.147+498A>T
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