Canonical Allele Identifier: CA10938843
Gene: MPL HGNC NCBI

Linked Data

ClinVar Variation Id: 1294122
ClinVar RCV Id: RCV001716028
dbSNP Id: rs710252
gnomAD v2: 1-43803222-G-A
gnomAD v3: 1-43337551-G-A
gnomAD v4: 1-43337551-G-A
MyVariant Identifiers: chr1:g.43803222G>A (hg19) chr1:g.43337551G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337551G>A , CM000663.2:g.43337551G>A GRCh38
NC_000001.10:g.43803222G>A , CM000663.1:g.43803222G>A GRCh37
NC_000001.9:g.43575809G>A NCBI36
NG_007525.1:g.4748G>A , LRG_510:g.4748G>A

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-298G>A XP_011539780.1:n.-298G>A
XM_017001320.1:c.-298G>A XP_016856809.1:n.-298G>A
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