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Canonical Allele Identifier:
CA862969331
Gene: CARM1P1
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.2982931T>G
GRCh37
chr9:g.2982931T>G
Linked Data - NCBI & NCI
dbSNP:
7044150
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.2982931T>G , CM000671.2:g.2982931T>G
GRCh38
NC_000009.11:g.2982931T>G , CM000671.1:g.2982931T>G
GRCh37
NC_000009.10:g.2972931T>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000426329.6:n.427+9532A>C
Search 100 bp 5'
Search 100 bp 3'