Canonical Allele Identifier: CA725975591
Gene: MYH3 HGNC NCBI

Linked Data

dbSNP Id: rs1302645810
gnomAD v4: 17-10639919-C-T
MyVariant Identifiers: chr17:g.10543236C>T (hg19) chr17:g.10639919C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639919C>T , CM000679.2:g.10639919C>T GRCh38
NC_000017.10:g.10543236C>T , CM000679.1:g.10543236C>T GRCh37
NC_000017.9:g.10483961C>T NCBI36
NG_011537.1:g.22380G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2682+77G>A MANE Select ENSP00000464317.1:n.2682+77G>A
ENST00000583535.5:c.2682+77G>A ENSP00000464317.1:n.2682+77G>A
NM_002470.3:c.2682+77G>A NP_002461.2:n.2682+77G>A
XM_011523870.1:c.2682+77G>A XP_011522172.1:n.2682+77G>A
XM_011523871.1:c.2682+77G>A XP_011522173.1:n.2682+77G>A
XM_011523872.1:c.2682+77G>A XP_011522174.1:n.2682+77G>A
XM_011523870.3:c.2682+77G>A XP_011522172.1:n.2682+77G>A
XM_011523871.2:c.2682+77G>A XP_011522173.1:n.2682+77G>A
NM_002470.4:c.2682+77G>A MANE Select NP_002461.2:n.2682+77G>A
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