Canonical Allele Identifier: CA806542
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs771652216
gnomAD v2: 1-43803488-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337817T>C , CM000663.2:g.43337817T>C GRCh38
NC_000001.10:g.43803488T>C , CM000663.1:g.43803488T>C GRCh37
NC_000001.9:g.43576075T>C NCBI36
NG_007525.1:g.5014T>C , LRG_510:g.5014T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372470.7:c.-32T>C ENSP00000361548.3:n.-32T>C
NM_005373.2:c.-32T>C , LRG_510t1:c.-32T>C NP_005364.1:n.-32T>C
XM_011541478.1:c.-32T>C XP_011539780.1:n.-32T>C
XM_017001320.1:c.-32T>C XP_016856809.1:n.-32T>C