Canonical Allele Identifier: CA883240702
Gene:

Linked Data

dbSNP Id: rs1312822502
gnomAD v3: 19-50837412-G-A
gnomAD v4: 19-50837412-G-A
MyVariant Identifiers: chr19:g.51340668G>A (hg19) chr19:g.50837412G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837412G>A , CM000681.2:g.50837412G>A GRCh38
NC_000019.9:g.51340668G>A , CM000681.1:g.51340668G>A GRCh37
NC_000019.8:g.56032480G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6119G>A
NR_131205.1:n.230+6119G>A
XR_936030.1:n.298+6119G>A
XR_936031.1:n.298+6119G>A
XR_936032.1:n.298+6119G>A
XR_936033.1:n.294+6119G>A
XR_936035.1:n.281+6119G>A
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