Canonical Allele Identifier: CA262352005

Gene:

Linked Data

• dbSNP Id: rs900297297
• MyVariant Identifiers: chr14:g.62968306A>T (hg19) ; chr14:g.62501588A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.62501588A>T , CM000676.2:g.62501588A>T	GRCh38
NC_000014.8:g.62968306A>T , CM000676.1:g.62968306A>T	GRCh37
NC_000014.7:g.62038059A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943932.1:n.116-2453A>T
XR_943932.2:n.103-2453A>T