Canonical Allele Identifier: CA8393364
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 321773
dbSNP Id: rs199513213

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10652520G>C , CM000679.2:g.10652520G>C GRCh38
NC_000017.10:g.10555837G>C , CM000679.1:g.10555837G>C GRCh37
NC_000017.9:g.10496562G>C NCBI36
NG_011537.1:g.9779C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.248C>G MANE Select ENSP00000464317.1:p.Pro83Arg
ENST00000582580.1:n.336C>G
ENST00000583535.5:c.248C>G ENSP00000464317.1:p.Pro83Arg
NM_002470.3:c.248C>G NP_002461.2:p.Pro83Arg
XM_011523870.1:c.248C>G XP_011522172.1:p.Pro83Arg
XM_011523871.1:c.248C>G XP_011522173.1:p.Pro83Arg
XM_011523872.1:c.248C>G XP_011522174.1:p.Pro83Arg
XM_011523870.3:c.248C>G XP_011522172.1:p.Pro83Arg
XM_011523871.2:c.248C>G XP_011522173.1:p.Pro83Arg
NM_002470.4:c.248C>G MANE Select NP_002461.2:p.Pro83Arg