Canonical Allele Identifier: CA680801445
Gene:

Linked Data

dbSNP Id: rs1022076894
MyVariant Identifiers: chr11:g.80562756C>G (hg19) chr11:g.80851713C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851713C>G , CM000673.2:g.80851713C>G GRCh38
NC_000011.9:g.80562756C>G , CM000673.1:g.80562756C>G GRCh37
NC_000011.8:g.80240404C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60578G>C
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