Canonical Allele Identifier: CA476840391
Gene:

Linked Data

MyVariant Identifiers: chr11:g.114231382T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114360660T>A , CM000673.2:g.114360660T>A GRCh38
NC_000011.9:g.114231382T>A , CM000673.1:g.114231382T>A GRCh37
NC_000011.8:g.113736592T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120567.1:n.3806A>T
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