Canonical Allele Identifier: CA611990020
Gene: PCCA-DT HGNC NCBI

Linked Data

dbSNP Id: rs1266877557
gnomAD v2: 13-100741190-C-T
gnomAD v4: 13-100088936-C-T
MyVariant Identifiers: chr13:g.100741190C>T (hg19) chr13:g.100088936C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100088936C>T , CM000675.2:g.100088936C>T GRCh38
NC_000013.10:g.100741190C>T , CM000675.1:g.100741190C>T GRCh37
NC_000013.9:g.99539191C>T NCBI36
NG_008768.1:g.4854C>T

Transcript Alleles

HGVS Amino-acid change
NR_132422.1:n.8G>A
Search 100 bp 5'
Search 100 bp 3'