Canonical Allele Identifier: CA10910901
Gene: PACERR HGNC NCBI

Linked Data

ClinVar Variation Id: 2571394
ClinVar RCV Id: RCV003312794
dbSNP Id: rs20417

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.186681189C>G , CM000663.2:g.186681189C>G GRCh38
NC_000001.10:g.186650321C>G , CM000663.1:g.186650321C>G GRCh37
NC_000001.9:g.184916944C>G NCBI36
NG_028206.2:g.4239G>C

Transcript Alleles

HGVS Amino-acid change
NR_125801.1:n.536C>G