Canonical Allele Identifier: CA1165575648
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1570463765

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337517T>C , CM000663.2:g.43337517T>C GRCh38
NC_000001.10:g.43803188T>C , CM000663.1:g.43803188T>C GRCh37
NC_000001.9:g.43575775T>C NCBI36
NG_007525.1:g.4714T>C , LRG_510:g.4714T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-332T>C XP_011539780.1:n.-332T>C
XM_017001320.1:c.-332T>C XP_016856809.1:n.-332T>C