Canonical Allele Identifier: CA13109889
Gene: CARM1P1 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.2982931T>C
GRCh37 chr9:g.2982931T>C
gnomAD v2:
9:2982931 T / C
gnomAD v3:
9:2982931 T / C
gnomAD v4:
chr9-2982931-T-C
Joint Max Group AF 0.94504628 (EAS)
Genomes Max Group AF 0.94504628 (EAS)
dbSNP:
7044150
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.2982931T>C , CM000671.2:g.2982931T>C GRCh38
NC_000009.11:g.2982931T>C , CM000671.1:g.2982931T>C GRCh37
NC_000009.10:g.2972931T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000426329.6:n.427+9532A>G
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