Canonical Allele Identifier: CA995983599
Gene: PCAT19 HGNC NCBI

Linked Data

dbSNP Id: rs2040502836
gnomAD v3: 19-41479685-T-C
gnomAD v4: 19-41479685-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41479685T>C , CM000681.2:g.41479685T>C GRCh38
NC_000019.8:g.46677433T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040109.1:n.950-401A>G
NR_040109.2:n.955-401A>G
NR_136334.1:n.67-401A>G
Search 100 bp 5'
Search 100 bp 3'