Canonical Allele Identifier: CA694169033
Gene: PCCA-DT HGNC NCBI

Linked Data

dbSNP Id: rs1357947134
gnomAD v3: 13-100088922-C-T
gnomAD v4: 13-100088922-C-T
MyVariant Identifiers: chr13:g.100741176C>T (hg19) chr13:g.100088922C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100088922C>T , CM000675.2:g.100088922C>T GRCh38
NC_000013.10:g.100741176C>T , CM000675.1:g.100741176C>T GRCh37
NC_000013.9:g.99539177C>T NCBI36
NG_008768.1:g.4840C>T

Transcript Alleles

HGVS Amino-acid change
NR_132422.1:n.22G>A
Search 100 bp 5'
Search 100 bp 3'