Canonical Allele Identifier: CA735989171
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1267613766
gnomAD v3: 1-43337545-A-G
gnomAD v4: 1-43337545-A-G
MyVariant Identifiers: chr1:g.43803216A>G (hg19) chr1:g.43337545A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337545A>G , CM000663.2:g.43337545A>G GRCh38
NC_000001.10:g.43803216A>G , CM000663.1:g.43803216A>G GRCh37
NC_000001.9:g.43575803A>G NCBI36
NG_007525.1:g.4742A>G , LRG_510:g.4742A>G

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-304A>G XP_011539780.1:n.-304A>G
XM_017001320.1:c.-304A>G XP_016856809.1:n.-304A>G
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