Canonical Allele Identifier: CA10910901
Gene: PACERR HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.186681189C>G
GRCh37 chr1:g.186650321C>G
gnomAD v2:
1:186650321 C / G
gnomAD v3:
1:186681189 C / G
gnomAD v4:
chr1-186681189-C-G
Joint Max Group AF 0.32914372 (AFR)
Genomes Max Group AF 0.32914372 (AFR)
ClinVar RCV:
RCV003312794
ClinVar Variation:
2571394
dbSNP:
20417
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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
Search 100 bp 5'
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