Canonical Allele Identifier: CA725975616

Gene: MYH3

Linked Data

• dbSNP Id: rs1202982807
• MyVariant Identifiers: chr17:g.10543276A>C (hg19) ; chr17:g.10639959A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639959A>C , CM000679.2:g.10639959A>C	GRCh38
NC_000017.10:g.10543276A>C , CM000679.1:g.10543276A>C	GRCh37
NC_000017.9:g.10484001A>C	NCBI36
NG_011537.1:g.22340T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2682+37T>G MANE Select	ENSP00000464317.1:n.2682+37T>G
ENST00000583535.5:c.2682+37T>G	ENSP00000464317.1:n.2682+37T>G
NM_002470.3:c.2682+37T>G	NP_002461.2:n.2682+37T>G
XM_011523870.1:c.2682+37T>G	XP_011522172.1:n.2682+37T>G
XM_011523871.1:c.2682+37T>G	XP_011522173.1:n.2682+37T>G
XM_011523872.1:c.2682+37T>G	XP_011522174.1:n.2682+37T>G
XM_011523870.3:c.2682+37T>G	XP_011522172.1:n.2682+37T>G
XM_011523871.2:c.2682+37T>G	XP_011522173.1:n.2682+37T>G
NM_002470.4:c.2682+37T>G MANE Select	NP_002461.2:n.2682+37T>G