Canonical Allele Identifier: CA398160788

Gene: MYH3

Linked Data

• dbSNP Id: rs1597486178
• MyVariant Identifiers: chr17:g.10543120C>T (hg19) ; chr17:g.10639803C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639803C>T , CM000679.2:g.10639803C>T	GRCh38
NC_000017.10:g.10543120C>T , CM000679.1:g.10543120C>T	GRCh37
NC_000017.9:g.10483845C>T	NCBI36
NG_011537.1:g.22496G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2683-1G>A MANE Select	ENSP00000464317.1:n.2683-1G>A
ENST00000583535.5:c.2683-1G>A	ENSP00000464317.1:n.2683-1G>A
NM_002470.3:c.2683-1G>A	NP_002461.2:n.2683-1G>A
XM_011523870.1:c.2683-1G>A	XP_011522172.1:n.2683-1G>A
XM_011523871.1:c.2683-1G>A	XP_011522173.1:n.2683-1G>A
XM_011523872.1:c.2683-1G>A	XP_011522174.1:n.2683-1G>A
XM_011523870.3:c.2683-1G>A	XP_011522172.1:n.2683-1G>A
XM_011523871.2:c.2683-1G>A	XP_011522173.1:n.2683-1G>A
NM_002470.4:c.2683-1G>A MANE Select	NP_002461.2:n.2683-1G>A