Canonical Allele Identifier: CA2625667531
Gene: NPC2 HGNC NCBI

Linked Data

gnomAD v4: 14-74493555-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74493555T>A , CM000676.2:g.74493555T>A GRCh38
NC_000014.8:g.74960258T>A , CM000676.1:g.74960258T>A GRCh37
NC_000014.7:g.74030011T>A NCBI36
NG_007117.1:g.4827A>T
NG_033074.1:g.4836T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000555592.1:c.-64+15A>T ENSP00000450887.1:n.-64+15A>T
ENST00000556009.5:c.147+476A>T
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