Canonical Allele Identifier: CA306408464
Gene:

Linked Data

dbSNP Id: rs916361320
MyVariant Identifiers: chr19:g.20218036C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20218036C>T , CM000681.2:g.20218036C>T GRCh38
NC_000019.9:g.20328845C>T , CM000681.1:g.20328845C>T GRCh37
NC_000019.8:g.20189845C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-720G>A
XR_936389.1:n.502-720G>A
XR_936390.1:n.511-720G>A
XR_936391.1:n.514-720G>A
XR_936392.1:n.514-720G>A
XR_936394.1:n.41-698C>T
XR_001754063.2:n.1506-720G>A
XR_001754064.2:n.138-720G>A
XR_001754066.1:n.3912-720G>A
XR_001754067.1:n.3912-720G>A
XR_001754068.1:n.3912-720G>A
XR_936394.2:n.41-698C>T
XR_936406.2:n.1411-720G>A
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