Canonical Allele Identifier: CA1165575699
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1647003054
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337665T>A , CM000663.2:g.43337665T>A GRCh38
NC_000001.10:g.43803336T>A , CM000663.1:g.43803336T>A GRCh37
NC_000001.9:g.43575923T>A NCBI36
NG_007525.1:g.4862T>A , LRG_510:g.4862T>A

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-184T>A XP_011539780.1:n.-184T>A
XM_017001320.1:c.-184T>A XP_016856809.1:n.-184T>A
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