Canonical Allele Identifier: CA806539
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs770784327
ExAC: 1:43803476 C / G
gnomAD v2: 1-43803476-C-G
gnomAD v4: 1-43337805-C-G
MyVariant Identifiers: chr1:g.43803476C>G (hg19) chr1:g.43337805C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337805C>G , CM000663.2:g.43337805C>G GRCh38
NC_000001.10:g.43803476C>G , CM000663.1:g.43803476C>G GRCh37
NC_000001.9:g.43576063C>G NCBI36
NG_007525.1:g.5002C>G , LRG_510:g.5002C>G

Transcript Alleles

HGVS Amino-acid Change
NM_005373.2:c.-44C>G , LRG_510t1:c.-44C>G NP_005364.1:n.-44C>G
XM_011541478.1:c.-44C>G XP_011539780.1:n.-44C>G
XM_017001320.1:c.-44C>G XP_016856809.1:n.-44C>G
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