Canonical Allele Identifier: CA21606661

Gene: MPL

Linked Data

• dbSNP Id: rs1029068556
• MyVariant Identifiers: chr1:g.43803400G>C (hg19) ; chr1:g.43337729G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.43337729G>C , CM000663.2:g.43337729G>C	GRCh38
NC_000001.10:g.43803400G>C , CM000663.1:g.43803400G>C	GRCh37
NC_000001.9:g.43575987G>C	NCBI36
NG_007525.1:g.4926G>C , LRG_510:g.4926G>C

Transcript Alleles

HGVS	Amino-acid Change
XM_011541478.1:c.-120G>C	XP_011539780.1:n.-120G>C
XM_017001320.1:c.-120G>C	XP_016856809.1:n.-120G>C