Canonical Allele Identifier: CA880474205
Gene:

Linked Data

dbSNP Id: rs1305692582
MyVariant Identifiers: chr19:g.20217935A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.20217935A>T , CM000681.2:g.20217935A>T GRCh38
NC_000019.9:g.20328744A>T , CM000681.1:g.20328744A>T GRCh37
NC_000019.8:g.20189744A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_936388.1:n.619-619T>A
XR_936389.1:n.502-619T>A
XR_936390.1:n.511-619T>A
XR_936391.1:n.514-619T>A
XR_936392.1:n.514-619T>A
XR_936394.1:n.41-799A>T
XR_001754063.2:n.1506-619T>A
XR_001754064.2:n.138-619T>A
XR_001754066.1:n.3912-619T>A
XR_001754067.1:n.3912-619T>A
XR_001754068.1:n.3912-619T>A
XR_936394.2:n.41-799A>T
XR_936406.2:n.1411-619T>A
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