Canonical Allele Identifier: CA51878428
Gene:

Linked Data

dbSNP Id: rs184028898
gnomAD v2: 2-88315955-G-C
gnomAD v3: 2-88016436-G-C
gnomAD v4: 2-88016436-G-C
MyVariant Identifiers: chr2:g.88315955G>C (hg19) chr2:g.88016436G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016436G>C , CM000664.2:g.88016436G>C GRCh38
NC_000002.11:g.88315955G>C , CM000664.1:g.88315955G>C GRCh37
NC_000002.10:g.88097070G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.781G>C
XR_940336.3:n.781G>C
Search 100 bp 5'
Search 100 bp 3'