Canonical Allele Identifier: CA486366300

Gene:

Linked Data

• MyVariant Identifiers: chr14:g.51323707T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50856989T>A , CM000676.2:g.50856989T>A	GRCh38
NC_000014.8:g.51323707T>A , CM000676.1:g.51323707T>A	GRCh37
NC_000014.7:g.50393457T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_943848.1:n.282+1109A>T
XR_943848.2:n.643+1109A>T