Canonical Allele Identifier: CA625036674

Gene: MYH3

Linked Data

• dbSNP Id: rs1266990727
• gnomAD v2: 17-10543279-G-A
• gnomAD v4: 17-10639962-G-A
• MyVariant Identifiers: chr17:g.10543279G>A (hg19) ; chr17:g.10639962G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639962G>A , CM000679.2:g.10639962G>A	GRCh38
NC_000017.10:g.10543279G>A , CM000679.1:g.10543279G>A	GRCh37
NC_000017.9:g.10484004G>A	NCBI36
NG_011537.1:g.22337C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000583535.6:c.2682+34C>T MANE Select	ENSP00000464317.1:n.2682+34C>T
ENST00000583535.5:c.2682+34C>T	ENSP00000464317.1:n.2682+34C>T
NM_002470.3:c.2682+34C>T	NP_002461.2:n.2682+34C>T
XM_011523870.1:c.2682+34C>T	XP_011522172.1:n.2682+34C>T
XM_011523871.1:c.2682+34C>T	XP_011522173.1:n.2682+34C>T
XM_011523872.1:c.2682+34C>T	XP_011522174.1:n.2682+34C>T
XM_011523870.3:c.2682+34C>T	XP_011522172.1:n.2682+34C>T
XM_011523871.2:c.2682+34C>T	XP_011522173.1:n.2682+34C>T
NM_002470.4:c.2682+34C>T MANE Select	NP_002461.2:n.2682+34C>T