Canonical Allele Identifier: CA894254628
Gene:

Linked Data

dbSNP Id: rs1271273085
gnomAD v3: 2-88016323-A-C
gnomAD v4: 2-88016323-A-C
MyVariant Identifiers: chr2:g.88315842A>C (hg19) chr2:g.88016323A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016323A>C , CM000664.2:g.88016323A>C GRCh38
NC_000002.11:g.88315842A>C , CM000664.1:g.88315842A>C GRCh37
NC_000002.10:g.88096957A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.668A>C
XR_940336.3:n.668A>C
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Search 100 bp 3'