Canonical Allele Identifier: CA476840372

Gene:

Linked Data

• MyVariant Identifiers: chr11:g.114231376A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.114360654A>C , CM000673.2:g.114360654A>C	GRCh38
NC_000011.9:g.114231376A>C , CM000673.1:g.114231376A>C	GRCh37
NC_000011.8:g.113736586A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_120567.1:n.3812T>G