Canonical Allele Identifier: CA2636109558

Gene: MYH3

Linked Data

• gnomAD v4: 17-10639905-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639905A>G , CM000679.2:g.10639905A>G	GRCh38
NC_000017.10:g.10543222A>G , CM000679.1:g.10543222A>G	GRCh37
NC_000017.9:g.10483947A>G	NCBI36
NG_011537.1:g.22394T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2682+91T>C MANE Select	ENSP00000464317.1:n.2682+91T>C
ENST00000583535.5:c.2682+91T>C	ENSP00000464317.1:n.2682+91T>C
NM_002470.3:c.2682+91T>C	NP_002461.2:n.2682+91T>C
XM_011523870.1:c.2682+91T>C	XP_011522172.1:n.2682+91T>C
XM_011523871.1:c.2682+91T>C	XP_011522173.1:n.2682+91T>C
XM_011523872.1:c.2682+91T>C	XP_011522174.1:n.2682+91T>C
XM_011523870.3:c.2682+91T>C	XP_011522172.1:n.2682+91T>C
XM_011523871.2:c.2682+91T>C	XP_011522173.1:n.2682+91T>C
NM_002470.4:c.2682+91T>C MANE Select	NP_002461.2:n.2682+91T>C