Canonical Allele Identifier: CA763641425
Gene:

Linked Data

dbSNP Id: rs890652446
MyVariant Identifiers: chr2:g.20685587A>C (hg19) chr2:g.20485826A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485826A>C , CM000664.2:g.20485826A>C GRCh38
NC_000002.11:g.20685587A>C , CM000664.1:g.20685587A>C GRCh37
NC_000002.10:g.20549068A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_157978.1:n.530+2912T>G
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