Canonical Allele Identifier: CA611990019
Gene: PCCA-DT HGNC NCBI

Linked Data

dbSNP Id: rs1033319038
gnomAD v2: 13-100741173-C-G
gnomAD v3: 13-100088919-C-G
gnomAD v4: 13-100088919-C-G
MyVariant Identifiers: chr13:g.100741173C>G (hg19) chr13:g.100088919C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.100088919C>G , CM000675.2:g.100088919C>G GRCh38
NC_000013.10:g.100741173C>G , CM000675.1:g.100741173C>G GRCh37
NC_000013.9:g.99539174C>G NCBI36
NG_008768.1:g.4837C>G

Transcript Alleles

HGVS Amino-acid change
NR_132422.1:n.25G>C
Search 100 bp 5'
Search 100 bp 3'