Canonical Allele Identifier: CA893591044
Gene:

Linked Data

dbSNP Id: rs1450494088
MyVariant Identifiers: chr2:g.81872971G>C (hg19) chr2:g.81645847G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.81645847G>C , CM000664.2:g.81645847G>C GRCh38
NC_000002.11:g.81872971G>C , CM000664.1:g.81872971G>C GRCh37
NC_000002.10:g.81726482G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940294.1:n.563+66238G>C
XR_940295.1:n.485+97100G>C
XR_001739571.1:n.485+97100G>C
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