Canonical Allele Identifier: CA232064540
Gene: CRACR2A HGNC NCBI

Linked Data

dbSNP Id: rs4268579
gnomAD v2: 12-3868079-T-C
gnomAD v3: 12-3758913-T-C
gnomAD v4: 12-3758913-T-C
MyVariant Identifiers: chr12:g.3868079T>C (hg19) chr12:g.3758913T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3758913T>C , CM000674.2:g.3758913T>C GRCh38
NC_000012.11:g.3868079T>C , CM000674.1:g.3868079T>C GRCh37
NC_000012.10:g.3738340T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000514026.2:n.255+5652A>G
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