Canonical Allele Identifier: CA398160641
Gene: MYH3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10639786A>G , CM000679.2:g.10639786A>G GRCh38
NC_000017.10:g.10543103A>G , CM000679.1:g.10543103A>G GRCh37
NC_000017.9:g.10483828A>G NCBI36
NG_011537.1:g.22513T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000583535.6:c.2699T>C MANE Select ENSP00000464317.1:p.Leu900Ser
ENST00000583535.5:c.2699T>C ENSP00000464317.1:p.Leu900Ser
NM_002470.3:c.2699T>C NP_002461.2:p.Leu900Ser
XM_011523870.1:c.2699T>C XP_011522172.1:p.Leu900Ser
XM_011523871.1:c.2699T>C XP_011522173.1:p.Leu900Ser
XM_011523872.1:c.2699T>C XP_011522174.1:p.Leu900Ser
XM_011523870.3:c.2699T>C XP_011522172.1:p.Leu900Ser
XM_011523871.2:c.2699T>C XP_011522173.1:p.Leu900Ser
NM_002470.4:c.2699T>C MANE Select NP_002461.2:p.Leu900Ser