Canonical Allele Identifier: CA1165575776
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1647004018
gnomAD v4: 1-43337816-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337816A>G , CM000663.2:g.43337816A>G GRCh38
NC_000001.10:g.43803487A>G , CM000663.1:g.43803487A>G GRCh37
NC_000001.9:g.43576074A>G NCBI36
NG_007525.1:g.5013A>G , LRG_510:g.5013A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.7:c.-33A>G ENSP00000361548.3:n.-33A>G
NM_005373.2:c.-33A>G , LRG_510t1:c.-33A>G NP_005364.1:n.-33A>G
XM_011541478.1:c.-33A>G XP_011539780.1:n.-33A>G
XM_017001320.1:c.-33A>G XP_016856809.1:n.-33A>G
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