Canonical Allele Identifier: CA398154300
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2896611
ClinVar RCV Id: RCV003730996
dbSNP Id: rs775785344

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639093T>C , CM000679.2:g.10639093T>C GRCh38
NC_000017.10:g.10542410T>C , CM000679.1:g.10542410T>C GRCh37
NC_000017.9:g.10483135T>C NCBI36
NG_011537.1:g.23206A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.3199A>G MANE Select ENSP00000464317.1:p.Ile1067Val
ENST00000583535.5:c.3199A>G ENSP00000464317.1:p.Ile1067Val
NM_002470.3:c.3199A>G NP_002461.2:p.Ile1067Val
XM_011523870.1:c.3199A>G XP_011522172.1:p.Ile1067Val
XM_011523871.1:c.3199A>G XP_011522173.1:p.Ile1067Val
XM_011523872.1:c.3199A>G XP_011522174.1:p.Ile1067Val
XM_011523870.3:c.3199A>G XP_011522172.1:p.Ile1067Val
XM_011523871.2:c.3199A>G XP_011522173.1:p.Ile1067Val
NM_002470.4:c.3199A>G MANE Select NP_002461.2:p.Ile1067Val