Canonical Allele Identifier: CA763555470
Gene:

Linked Data

dbSNP Id: rs1327119674
MyVariant Identifiers: chr2:g.204799403C>G (hg19) chr2:g.203934680C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934680C>G , CM000664.2:g.203934680C>G GRCh38
NC_000002.11:g.204799403C>G , CM000664.1:g.204799403C>G GRCh37
NC_000002.10:g.204507648C>G NCBI36
NG_011586.1:g.2901C>G , LRG_65:g.2901C>G

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1428G>C
XR_001739861.1:n.1588G>C
XR_427213.3:n.474+1428G>C
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