Canonical Allele Identifier: CA497979141

Gene: MYH3

Linked Data

• MyVariant Identifiers: chr17:g.10542886T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.10639569T>G , CM000679.2:g.10639569T>G	GRCh38
NC_000017.10:g.10542886T>G , CM000679.1:g.10542886T>G	GRCh37
NC_000017.9:g.10483611T>G	NCBI36
NG_011537.1:g.22730A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000583535.6:c.2916A>C MANE Select	ENSP00000464317.1:p.Thr972=
ENST00000583535.5:c.2916A>C	ENSP00000464317.1:p.Thr972=
NM_002470.3:c.2916A>C	NP_002461.2:p.Thr972=
XM_011523870.1:c.2916A>C	XP_011522172.1:p.Thr972=
XM_011523871.1:c.2916A>C	XP_011522173.1:p.Thr972=
XM_011523872.1:c.2916A>C	XP_011522174.1:p.Thr972=
XM_011523870.3:c.2916A>C	XP_011522172.1:p.Thr972=
XM_011523871.2:c.2916A>C	XP_011522173.1:p.Thr972=
NM_002470.4:c.2916A>C MANE Select	NP_002461.2:p.Thr972=