Canonical Allele Identifier: CA232064544
Gene: CRACR2A HGNC NCBI

Linked Data

dbSNP Id: rs532378598
gnomAD v2: 12-3868102-C-G
gnomAD v3: 12-3758936-C-G
gnomAD v4: 12-3758936-C-G
MyVariant Identifiers: chr12:g.3868102C>G (hg19) chr12:g.3758936C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.3758936C>G , CM000674.2:g.3758936C>G GRCh38
NC_000012.11:g.3868102C>G , CM000674.1:g.3868102C>G GRCh37
NC_000012.10:g.3738363C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000514026.2:n.255+5629G>C
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