Canonical Allele Identifier: CA725975671
Gene: MYH3 HGNC NCBI

Linked Data

dbSNP Id: rs1384042436
MyVariant Identifiers: chr17:g.10543283A>T (hg19) chr17:g.10639966A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639966A>T , CM000679.2:g.10639966A>T GRCh38
NC_000017.10:g.10543283A>T , CM000679.1:g.10543283A>T GRCh37
NC_000017.9:g.10484008A>T NCBI36
NG_011537.1:g.22333T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000583535.6:c.2682+30T>A MANE Select ENSP00000464317.1:n.2682+30T>A
ENST00000583535.5:c.2682+30T>A ENSP00000464317.1:n.2682+30T>A
NM_002470.3:c.2682+30T>A NP_002461.2:n.2682+30T>A
XM_011523870.1:c.2682+30T>A XP_011522172.1:n.2682+30T>A
XM_011523871.1:c.2682+30T>A XP_011522173.1:n.2682+30T>A
XM_011523872.1:c.2682+30T>A XP_011522174.1:n.2682+30T>A
XM_011523870.3:c.2682+30T>A XP_011522172.1:n.2682+30T>A
XM_011523871.2:c.2682+30T>A XP_011522173.1:n.2682+30T>A
NM_002470.4:c.2682+30T>A MANE Select NP_002461.2:n.2682+30T>A
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