Canonical Allele Identifier: CA257451218
Gene:

Linked Data

dbSNP Id: rs886142308
MyVariant Identifiers: chr14:g.20793468T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793468T>A , CM000676.2:g.20793468T>A GRCh38
NC_000014.8:g.21261627T>A , CM000676.1:g.21261627T>A GRCh37
NC_000014.7:g.20331467T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+682T>A
XR_943585.1:n.585+682T>A
XR_001750620.1:n.3271+682T>A
XR_001750621.1:n.3271+682T>A
XR_001750622.1:n.637+6436A>T
XR_001750623.1:n.637+6436A>T
XR_001750624.1:n.637+6436A>T