Canonical Allele Identifier: CA21606637
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1045639700
gnomAD v2: 1-43803293-C-T
gnomAD v3: 1-43337622-C-T
gnomAD v4: 1-43337622-C-T
MyVariant Identifiers: chr1:g.43803293C>T (hg19) chr1:g.43337622C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337622C>T , CM000663.2:g.43337622C>T GRCh38
NC_000001.10:g.43803293C>T , CM000663.1:g.43803293C>T GRCh37
NC_000001.9:g.43575880C>T NCBI36
NG_007525.1:g.4819C>T , LRG_510:g.4819C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-227C>T XP_011539780.1:n.-227C>T
XM_017001320.1:c.-227C>T XP_016856809.1:n.-227C>T
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