Canonical Allele Identifier: CA16343926
Gene: NACA4P HGNC NCBI

Linked Data

dbSNP Id: rs16867579
gnomAD v2: 8-102375267-A-C
gnomAD v3: 8-101363039-A-C
gnomAD v4: 8-101363039-A-C
MyVariant Identifiers: chr8:g.102375267A>C (hg19) chr8:g.101363039A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.101363039A>C , CM000670.2:g.101363039A>C GRCh38
NC_000008.10:g.102375267A>C , CM000670.1:g.102375267A>C GRCh37
NC_000008.9:g.102444443A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000419462.1:n.285+961A>C
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