Canonical Allele Identifier: CA398160229

Gene: MYH3

Linked Data

• dbSNP Id: rs2074250740
• MyVariant Identifiers: chr17:g.10543056G>A (hg19) ; chr17:g.10639739G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639739G>A , CM000679.2:g.10639739G>A	GRCh38
NC_000017.10:g.10543056G>A , CM000679.1:g.10543056G>A	GRCh37
NC_000017.9:g.10483781G>A	NCBI36
NG_011537.1:g.22560C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2746C>T MANE Select	ENSP00000464317.1:p.Leu916Phe
ENST00000583535.5:c.2746C>T	ENSP00000464317.1:p.Leu916Phe
NM_002470.3:c.2746C>T	NP_002461.2:p.Leu916Phe
XM_011523870.1:c.2746C>T	XP_011522172.1:p.Leu916Phe
XM_011523871.1:c.2746C>T	XP_011522173.1:p.Leu916Phe
XM_011523872.1:c.2746C>T	XP_011522174.1:p.Leu916Phe
XM_011523870.3:c.2746C>T	XP_011522172.1:p.Leu916Phe
XM_011523871.2:c.2746C>T	XP_011522173.1:p.Leu916Phe
NM_002470.4:c.2746C>T MANE Select	NP_002461.2:p.Leu916Phe