Canonical Allele Identifier: CA476840463
Gene:

Linked Data

MyVariant Identifiers: chr11:g.114231403T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114360681T>G , CM000673.2:g.114360681T>G GRCh38
NC_000011.9:g.114231403T>G , CM000673.1:g.114231403T>G GRCh37
NC_000011.8:g.113736613T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120567.1:n.3785A>C
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