Canonical Allele Identifier: CA309668920
Gene:

Linked Data

dbSNP Id: rs561926282
gnomAD v3: 19-50837454-T-A
gnomAD v4: 19-50837454-T-A
MyVariant Identifiers: chr19:g.51340710T>A (hg19) chr19:g.50837454T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837454T>A , CM000681.2:g.50837454T>A GRCh38
NC_000019.9:g.51340710T>A , CM000681.1:g.51340710T>A GRCh37
NC_000019.8:g.56032522T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131203.1:n.213+6161T>A
NR_131205.1:n.230+6161T>A
XR_936030.1:n.298+6161T>A
XR_936031.1:n.298+6161T>A
XR_936032.1:n.298+6161T>A
XR_936033.1:n.294+6161T>A
XR_936035.1:n.281+6161T>A
Search 100 bp 5'
Search 100 bp 3'