Canonical Allele Identifier: CA476840380
Gene:

Linked Data

MyVariant Identifiers: chr11:g.114231378T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114360656T>G , CM000673.2:g.114360656T>G GRCh38
NC_000011.9:g.114231378T>G , CM000673.1:g.114231378T>G GRCh37
NC_000011.8:g.113736588T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120567.1:n.3810A>C
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