Canonical Allele Identifier: CA735989265
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1179001857
MyVariant Identifiers: chr1:g.43803273C>A (hg19) chr1:g.43337602C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337602C>A , CM000663.2:g.43337602C>A GRCh38
NC_000001.10:g.43803273C>A , CM000663.1:g.43803273C>A GRCh37
NC_000001.9:g.43575860C>A NCBI36
NG_007525.1:g.4799C>A , LRG_510:g.4799C>A

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-247C>A XP_011539780.1:n.-247C>A
XM_017001320.1:c.-247C>A XP_016856809.1:n.-247C>A
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