Canonical Allele Identifier: CA476840440
Gene:

Linked Data

MyVariant Identifiers: chr11:g.114231397A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.114360675A>C , CM000673.2:g.114360675A>C GRCh38
NC_000011.9:g.114231397A>C , CM000673.1:g.114231397A>C GRCh37
NC_000011.8:g.113736607A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120567.1:n.3791T>G