Canonical Allele Identifier: CA21606590
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs181724591
gnomAD v3: 1-43337521-A-G
gnomAD v4: 1-43337521-A-G
MyVariant Identifiers: chr1:g.43803192A>G (hg19) chr1:g.43337521A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337521A>G , CM000663.2:g.43337521A>G GRCh38
NC_000001.10:g.43803192A>G , CM000663.1:g.43803192A>G GRCh37
NC_000001.9:g.43575779A>G NCBI36
NG_007525.1:g.4718A>G , LRG_510:g.4718A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-328A>G XP_011539780.1:n.-328A>G
XM_017001320.1:c.-328A>G XP_016856809.1:n.-328A>G
Search 100 bp 5'
Search 100 bp 3'