Canonical Allele Identifier: CA21606673
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs1033242020
gnomAD v3: 1-43337748-G-C
gnomAD v4: 1-43337748-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337748G>C , CM000663.2:g.43337748G>C GRCh38
NC_000001.10:g.43803419G>C , CM000663.1:g.43803419G>C GRCh37
NC_000001.9:g.43576006G>C NCBI36
NG_007525.1:g.4945G>C , LRG_510:g.4945G>C

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-101G>C XP_011539780.1:n.-101G>C
XM_017001320.1:c.-101G>C XP_016856809.1:n.-101G>C