Canonical Allele Identifier: CA265876943

Gene:

Linked Data

• dbSNP Id: rs373764430
• MyVariant Identifiers: chr14:g.95078577A>T (hg19) ; chr14:g.94612240A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94612240A>T , CM000676.2:g.94612240A>T	GRCh38
NC_000014.8:g.95078577A>T , CM000676.1:g.95078577A>T	GRCh37
NC_000014.7:g.94148330A>T	NCBI36
NG_012879.1:g.4864A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000553947.1:c.805-57A>T