Canonical Allele Identifier: CA476840425
Gene:

Linked Data

MyVariant Identifiers: chr11:g.114231392A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114360670A>C , CM000673.2:g.114360670A>C GRCh38
NC_000011.9:g.114231392A>C , CM000673.1:g.114231392A>C GRCh37
NC_000011.8:g.113736602A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120567.1:n.3796T>G