Canonical Allele Identifier: CA2247317230
Gene: MYH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639937T= , CM000679.2:g.10639937T= GRCh38
NC_000017.10:g.10543254T= , CM000679.1:g.10543254T= GRCh37
NC_000017.9:g.10483979T= NCBI36
NG_011537.1:g.22362A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2682+59A= MANE Select ENSP00000464317.1:n.2682+59A=
ENST00000583535.5:c.2682+59A= ENSP00000464317.1:n.2682+59A=
NM_002470.3:c.2682+59A= NP_002461.2:n.2682+59A=
XM_011523870.1:c.2682+59A= XP_011522172.1:n.2682+59A=
XM_011523871.1:c.2682+59A= XP_011522173.1:n.2682+59A=
XM_011523872.1:c.2682+59A= XP_011522174.1:n.2682+59A=
XM_011523870.3:c.2682+59A= XP_011522172.1:n.2682+59A=
XM_011523871.2:c.2682+59A= XP_011522173.1:n.2682+59A=
NM_002470.4:c.2682+59A= MANE Select NP_002461.2:n.2682+59A=
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