Canonical Allele Identifier: CA735989261
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1407240397
MyVariant Identifiers: chr1:g.43803263G>C (hg19) chr1:g.43337592G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337592G>C , CM000663.2:g.43337592G>C GRCh38
NC_000001.10:g.43803263G>C , CM000663.1:g.43803263G>C GRCh37
NC_000001.9:g.43575850G>C NCBI36
NG_007525.1:g.4789G>C , LRG_510:g.4789G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-257G>C XP_011539780.1:n.-257G>C
XM_017001320.1:c.-257G>C XP_016856809.1:n.-257G>C
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