Canonical Allele Identifier: CA21606716
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs867328605
MyVariant Identifiers: chr1:g.43803508G>A (hg19) chr1:g.43337837G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337837G>A , CM000663.2:g.43337837G>A GRCh38
NC_000001.10:g.43803508G>A , CM000663.1:g.43803508G>A GRCh37
NC_000001.9:g.43576095G>A NCBI36
NG_007525.1:g.5034G>A , LRG_510:g.5034G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.-12G>A MANE Select ENSP00000361548.3:n.-12G>A
ENST00000372470.7:c.-12G>A ENSP00000361548.3:n.-12G>A
NM_005373.2:c.-12G>A , LRG_510t1:c.-12G>A NP_005364.1:n.-12G>A
XM_011541478.1:c.-12G>A XP_011539780.1:n.-12G>A
XM_017001320.1:c.-12G>A XP_016856809.1:n.-12G>A
NM_005373.3:c.-12G>A MANE Select NP_005364.1:n.-12G>A
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