Canonical Allele Identifier: CA704082189
Gene:

Linked Data

dbSNP Id: rs1210664300
gnomAD v3: 14-20793448-A-T
gnomAD v4: 14-20793448-A-T
MyVariant Identifiers: chr14:g.21261607A>T (hg19) chr14:g.20793448A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793448A>T , CM000676.2:g.20793448A>T GRCh38
NC_000014.8:g.21261607A>T , CM000676.1:g.21261607A>T GRCh37
NC_000014.7:g.20331447A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+662A>T
XR_943585.1:n.585+662A>T
XR_001750620.1:n.3271+662A>T
XR_001750621.1:n.3271+662A>T
XR_001750622.1:n.637+6456T>A
XR_001750623.1:n.637+6456T>A
XR_001750624.1:n.637+6456T>A
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