Canonical Allele Identifier: CA2695812950
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs2153920165
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43352775A>G , CM000663.2:g.43352775A>G GRCh38
NC_000001.10:g.43818446A>G , CM000663.1:g.43818446A>G GRCh37
NC_000001.9:g.43591033A>G NCBI36
NG_007525.1:g.19972A>G , LRG_510:g.19972A>G

Transcript Alleles

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