Allele Registry

Canonical Allele Identifier: CA308399655

Gene: PCAT19 HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chr19:g.41479679G>A

Linked Data - Sequence & Population

gnomAD v3:

19:41479679 G / A

gnomAD v4:

chr19-41479679-G-A

Joint Max Group AF 0.79055906 (AFR)

Genomes Max Group AF 0.79055906 (AFR)

Linked Data - NCBI & NCI

dbSNP:

11672691

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41479679G>A , CM000681.2:g.41479679G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
NR_040109.1:n.950-395C>T
NR_040109.2:n.955-395C>T
NR_136334.1:n.67-395C>T

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