Allele Registry

Canonical Allele Identifier: CA168261863

Gene: EPHA1-AS1 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chr7:g.143425831A>C

GRCh37 chr7:g.143122924A>C

Linked Data - Sequence & Population

gnomAD v2:

7:143122924 A / C

gnomAD v3:

7:143425831 A / C

gnomAD v4:

chr7-143425831-A-C

Joint Max Group AF 0.09160902 (NFE)

Genomes Max Group AF 0.09160902 (NFE)

Linked Data - NCBI & NCI

dbSNP:

78571833

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.143425831A>C , CM000669.2:g.143425831A>C	GRCh38
NC_000007.13:g.143122924A>C , CM000669.1:g.143122924A>C	GRCh37
NC_000007.12:g.142833046A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_033897.1:n.206+10632A>C

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