Canonical Allele Identifier: CA522806054
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs771652216
gnomAD v2: 1-43803488-T-G
gnomAD v4: 1-43337817-T-G
MyVariant Identifiers: chr1:g.43803488T>G (hg19) chr1:g.43337817T>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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