Allele Registry

Canonical Allele Identifier: CA16343926

Gene: NACA4P HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr8:g.101363039A>C

GRCh37 chr8:g.102375267A>C

Linked Data - Sequence & Population

gnomAD v2:

8:102375267 A / C

gnomAD v3:

8:101363039 A / C

gnomAD v4:

chr8-101363039-A-C

Joint Max Group AF 0.33900466 (AFR)

Genomes Max Group AF 0.33900466 (AFR)

Linked Data - NCBI & NCI

dbSNP:

16867579

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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