Canonical Allele Identifier: CA761272646
Gene:

Linked Data

dbSNP Id: rs1309583160
MyVariant Identifiers: chr2:g.18025216C>G (hg19) chr2:g.17843949C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.17843949C>G , CM000664.2:g.17843949C>G GRCh38
NC_000002.11:g.18025216C>G , CM000664.1:g.18025216C>G GRCh37
NC_000002.10:g.17888697C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939764.2:n.447+3745G>C
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