Canonical Allele Identifier: CA11098119
Gene:

Linked Data

dbSNP Id: rs13403276
gnomAD v2: 2-219081297-T-C
gnomAD v3: 2-218216574-T-C
gnomAD v4: 2-218216574-T-C
MyVariant Identifiers: chr2:g.219081297T>C (hg19) chr2:g.218216574T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.218216574T>C , CM000664.2:g.218216574T>C GRCh38
NC_000002.11:g.219081297T>C , CM000664.1:g.219081297T>C GRCh37
NC_000002.10:g.218789542T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_241416.2:n.371A>G
XR_923908.1:n.368A>G
Search 100 bp 5'
Search 100 bp 3'