Canonical Allele Identifier: CA707588607

Gene:

Linked Data

• dbSNP Id: rs1483391653
• gnomAD v3: 14-62501732-G-T
• gnomAD v4: 14-62501732-G-T
• MyVariant Identifiers: chr14:g.62968450G>T (hg19) ; chr14:g.62501732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.62501732G>T , CM000676.2:g.62501732G>T	GRCh38
NC_000014.8:g.62968450G>T , CM000676.1:g.62968450G>T	GRCh37
NC_000014.7:g.62038203G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_943932.1:n.116-2309G>T
XR_943932.2:n.103-2309G>T