Canonical Allele Identifier: CA15807252
Gene:

Linked Data

dbSNP Id: rs11156672
gnomAD v2: 14-21261605-T-C
gnomAD v3: 14-20793446-T-C
gnomAD v4: 14-20793446-T-C
MyVariant Identifiers: chr14:g.21261605T>C (hg19) chr14:g.20793446T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20793446T>C , CM000676.2:g.20793446T>C GRCh38
NC_000014.8:g.21261605T>C , CM000676.1:g.21261605T>C GRCh37
NC_000014.7:g.20331445T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943584.1:n.585+660T>C
XR_943585.1:n.585+660T>C
XR_001750620.1:n.3271+660T>C
XR_001750621.1:n.3271+660T>C
XR_001750622.1:n.637+6458A>G
XR_001750623.1:n.637+6458A>G
XR_001750624.1:n.637+6458A>G
Search 100 bp 5'
Search 100 bp 3'