ClinGen Allele Registry
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Canonical Allele Identifier:
CA862969238
Gene: CARM1P1
HGNC
NCBI
Linked Data
dbSNP Id:
rs1413867906
gnomAD v3:
9-2982857-T-C
gnomAD v4:
9-2982857-T-C
MyVariant Identifiers:
chr9:g.2982857T>C (hg19)
chr9:g.2982857T>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.2982857T>C , CM000671.2:g.2982857T>C
GRCh38
NC_000009.11:g.2982857T>C , CM000671.1:g.2982857T>C
GRCh37
NC_000009.10:g.2972857T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000426329.6:n.427+9606A>G
Search 100 bp 5'
Search 100 bp 3'