Canonical Allele Identifier: CA2645221655
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs2153916081
gnomAD v4: 1-43337828-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337828A>T , CM000663.2:g.43337828A>T GRCh38
NC_000001.10:g.43803499A>T , CM000663.1:g.43803499A>T GRCh37
NC_000001.9:g.43576086A>T NCBI36
NG_007525.1:g.5025A>T , LRG_510:g.5025A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.9:c.-21A>T MANE Select ENSP00000361548.3:n.-21A>T
ENST00000372470.7:c.-21A>T ENSP00000361548.3:n.-21A>T
NM_005373.2:c.-21A>T , LRG_510t1:c.-21A>T NP_005364.1:n.-21A>T
XM_011541478.1:c.-21A>T XP_011539780.1:n.-21A>T
XM_017001320.1:c.-21A>T XP_016856809.1:n.-21A>T
NM_005373.3:c.-21A>T MANE Select NP_005364.1:n.-21A>T