Canonical Allele Identifier: CA522507540
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1182904739
gnomAD v2: 1-43803373-G-C
gnomAD v3: 1-43337702-G-C
gnomAD v4: 1-43337702-G-C
MyVariant Identifiers: chr1:g.43803373G>C (hg19) chr1:g.43337702G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337702G>C , CM000663.2:g.43337702G>C GRCh38
NC_000001.10:g.43803373G>C , CM000663.1:g.43803373G>C GRCh37
NC_000001.9:g.43575960G>C NCBI36
NG_007525.1:g.4899G>C , LRG_510:g.4899G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-147G>C XP_011539780.1:n.-147G>C
XM_017001320.1:c.-147G>C XP_016856809.1:n.-147G>C
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