Canonical Allele Identifier: CA625032239
Gene: MYH3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3023560
ClinVar RCV Id: RCV003880655
dbSNP Id: rs1402850885
gnomAD v2: 17-10542874-T-C
gnomAD v3: 17-10639557-T-C
gnomAD v4: 17-10639557-T-C
MyVariant Identifiers: chr17:g.10542874T>C (hg19) chr17:g.10639557T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639557T>C , CM000679.2:g.10639557T>C GRCh38
NC_000017.10:g.10542874T>C , CM000679.1:g.10542874T>C GRCh37
NC_000017.9:g.10483599T>C NCBI36
NG_011537.1:g.22742A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2925+3A>G MANE Select ENSP00000464317.1:n.2925+3A>G
ENST00000583535.5:c.2925+3A>G ENSP00000464317.1:n.2925+3A>G
NM_002470.3:c.2925+3A>G NP_002461.2:n.2925+3A>G
XM_011523870.1:c.2925+3A>G XP_011522172.1:n.2925+3A>G
XM_011523871.1:c.2925+3A>G XP_011522173.1:n.2925+3A>G
XM_011523872.1:c.2925+3A>G XP_011522174.1:n.2925+3A>G
XM_011523870.3:c.2925+3A>G XP_011522172.1:n.2925+3A>G
XM_011523871.2:c.2925+3A>G XP_011522173.1:n.2925+3A>G
NM_002470.4:c.2925+3A>G MANE Select NP_002461.2:n.2925+3A>G
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