Canonical Allele Identifier: CA10688575
Gene: CRPP1 HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.159705143C>T
GRCh37 chr1:g.159674933C>T
gnomAD v2:
1:159674933 C / T
gnomAD v3:
1:159705143 C / T
gnomAD v4:
chr1-159705143-C-T
Joint Max Group AF 0.57357377 (EAS)
Genomes Max Group AF 0.55845923 (EAS)
Exomes Max Group AF 0.58000648 (EAS)
dbSNP:
876537
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159705143C>T , CM000663.2:g.159705143C>T GRCh38
NC_000001.10:g.159674933C>T , CM000663.1:g.159674933C>T GRCh37
NC_000001.9:g.157941557C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000412857.1:n.465G>A
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