Canonical Allele Identifier: CA632429698
Gene:

Linked Data

dbSNP Id: rs1331750010
gnomAD v2: 19-20329182-G-A
gnomAD v3: 19-20218373-G-A
gnomAD v4: 19-20218373-G-A
MyVariant Identifiers: chr19:g.20329182G>A (hg19) chr19:g.20218373G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218373G>A , CM000681.2:g.20218373G>A GRCh38
NC_000019.9:g.20329182G>A , CM000681.1:g.20329182G>A GRCh37
NC_000019.8:g.20190182G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-1057C>T
XR_936389.1:n.502-1057C>T
XR_936390.1:n.511-1057C>T
XR_936391.1:n.514-1057C>T
XR_936392.1:n.514-1057C>T
XR_936394.1:n.41-361G>A
XR_001754063.2:n.1506-1057C>T
XR_001754064.2:n.138-1057C>T
XR_001754066.1:n.3912-1057C>T
XR_001754067.1:n.3912-1057C>T
XR_001754068.1:n.3912-1057C>T
XR_936394.2:n.41-361G>A
XR_936406.2:n.1411-1057C>T
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