Canonical Allele Identifier: CA21606657
Gene: MPL HGNC NCBI

Linked Data

dbSNP Id: rs887909846
gnomAD v2: 1-43803396-C-T
gnomAD v3: 1-43337725-C-T
gnomAD v4: 1-43337725-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.43337725C>T , CM000663.2:g.43337725C>T GRCh38
NC_000001.10:g.43803396C>T , CM000663.1:g.43803396C>T GRCh37
NC_000001.9:g.43575983C>T NCBI36
NG_007525.1:g.4922C>T , LRG_510:g.4922C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011541478.1:c.-124C>T XP_011539780.1:n.-124C>T
XM_017001320.1:c.-124C>T XP_016856809.1:n.-124C>T