Canonical Allele Identifier: CA398156935
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2293655
ClinVar RCV Id: RCV002841700
dbSNP Id: rs1436860220
gnomAD v3: 17-10639618-T-G
gnomAD v4: 17-10639618-T-G
MyVariant Identifiers: chr17:g.10542935T>G (hg19) chr17:g.10639618T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639618T>G , CM000679.2:g.10639618T>G GRCh38
NC_000017.10:g.10542935T>G , CM000679.1:g.10542935T>G GRCh37
NC_000017.9:g.10483660T>G NCBI36
NG_011537.1:g.22681A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2867A>C MANE Select ENSP00000464317.1:p.Asp956Ala
ENST00000583535.5:c.2867A>C ENSP00000464317.1:p.Asp956Ala
NM_002470.3:c.2867A>C NP_002461.2:p.Asp956Ala
XM_011523870.1:c.2867A>C XP_011522172.1:p.Asp956Ala
XM_011523871.1:c.2867A>C XP_011522173.1:p.Asp956Ala
XM_011523872.1:c.2867A>C XP_011522174.1:p.Asp956Ala
XM_011523870.3:c.2867A>C XP_011522172.1:p.Asp956Ala
XM_011523871.2:c.2867A>C XP_011522173.1:p.Asp956Ala
NM_002470.4:c.2867A>C MANE Select NP_002461.2:p.Asp956Ala
Search 100 bp 5'
Search 100 bp 3'