Canonical Allele Identifier: CA8392684
Gene: MYH3 HGNC NCBI

Linked Data

dbSNP Id: rs575887424
ExAC: 17:10543051 C / T
gnomAD v2: 17-10543051-C-T
gnomAD v3: 17-10639734-C-T
gnomAD v4: 17-10639734-C-T
MyVariant Identifiers: chr17:g.10543051C>T (hg19) chr17:g.10639734C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639734C>T , CM000679.2:g.10639734C>T GRCh38
NC_000017.10:g.10543051C>T , CM000679.1:g.10543051C>T GRCh37
NC_000017.9:g.10483776C>T NCBI36
NG_011537.1:g.22565G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2751G>A MANE Select ENSP00000464317.1:p.Glu917=
ENST00000583535.5:c.2751G>A ENSP00000464317.1:p.Glu917=
NM_002470.3:c.2751G>A NP_002461.2:p.Glu917=
XM_011523870.1:c.2751G>A XP_011522172.1:p.Glu917=
XM_011523871.1:c.2751G>A XP_011522173.1:p.Glu917=
XM_011523872.1:c.2751G>A XP_011522174.1:p.Glu917=
XM_011523870.3:c.2751G>A XP_011522172.1:p.Glu917=
XM_011523871.2:c.2751G>A XP_011522173.1:p.Glu917=
NM_002470.4:c.2751G>A MANE Select NP_002461.2:p.Glu917=
Search 100 bp 5'
Search 100 bp 3'