Canonical Allele Identifier: CA735989175
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1181864003
MyVariant Identifiers: chr1:g.43803217T>C (hg19) chr1:g.43337546T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337546T>C , CM000663.2:g.43337546T>C GRCh38
NC_000001.10:g.43803217T>C , CM000663.1:g.43803217T>C GRCh37
NC_000001.9:g.43575804T>C NCBI36
NG_007525.1:g.4743T>C , LRG_510:g.4743T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-303T>C XP_011539780.1:n.-303T>C
XM_017001320.1:c.-303T>C XP_016856809.1:n.-303T>C
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